Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001161009.2 | 534 | Intron | NP_001154481.1 | ||
NM_001161010.2 | 534 | Missense Mutation | GCC,TCC | A48S | NP_001154482.1 |
NM_001161011.2 | 534 | Intron | NP_001154483.1 | ||
NM_001161012.2 | 534 | Intron | NP_001154484.1 | ||
NM_001161013.2 | 534 | Intron | NP_001154485.1 | ||
NM_031905.4 | 534 | Missense Mutation | GCC,TCC | A48S | NP_114111.2 |
XM_005250628.2 | 534 | Missense Mutation | GCC,TCC | A48S | XP_005250685.1 |
XM_011516601.2 | 534 | Intron | XP_011514903.1 | ||
XM_011516602.2 | 534 | Intron | XP_011514904.1 | ||
XM_017012684.1 | 534 | Missense Mutation | GCC,TCC | A48S | XP_016868173.1 |
XM_017012685.1 | 534 | Missense Mutation | GCC,TCC | A48S | XP_016868174.1 |
XM_017012686.1 | 534 | Missense Mutation | GCC,TCC | A48S | XP_016868175.1 |
XM_017012687.1 | 534 | Intron | XP_016868176.1 | ||
XM_017012688.1 | 534 | Missense Mutation | GCC,TCC | A48S | XP_016868177.1 |
XM_017012689.1 | 534 | Missense Mutation | GCC,TCC | A48S | XP_016868178.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001111038.1 | 534 | Intron | NP_001104508.1 | ||
NM_001287150.1 | 534 | Intron | NP_001274079.1 | ||
NM_145032.3 | 534 | Intron | NP_659469.3 | ||
XM_005250205.3 | 534 | Intron | XP_005250262.1 | ||
XM_005250207.3 | 534 | Intron | XP_005250264.1 | ||
XM_005250208.3 | 534 | Intron | XP_005250265.1 | ||
XM_005250209.2 | 534 | Intron | XP_005250266.1 | ||
XM_006715898.2 | 534 | Intron | XP_006715961.1 | ||
XM_011515928.2 | 534 | Intron | XP_011514230.1 | ||
XM_011515929.2 | 534 | Intron | XP_011514231.1 | ||
XM_011515930.2 | 534 | Intron | XP_011514232.1 | ||
XM_011515932.2 | 534 | Intron | XP_011514234.1 | ||
XM_017011850.1 | 534 | Intron | XP_016867339.1 | ||
XM_017011851.1 | 534 | Intron | XP_016867340.1 | ||
XM_017011852.1 | 534 | Intron | XP_016867341.1 | ||
XM_017011853.1 | 534 | Intron | XP_016867342.1 |