Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001171747.1 | 613 | Intron | NP_001165218.1 | ||
NM_024616.2 | 613 | Intron | NP_078892.2 | ||
XM_011513133.2 | 613 | Intron | XP_011511435.1 | ||
XM_017007181.1 | 613 | Intron | XP_016862670.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001190259.1 | 613 | Missense Mutation | CGT,TGT | R167C | NP_001177188.1 |
NM_001190260.1 | 613 | Missense Mutation | CGT,TGT | R150C | NP_001177189.1 |
NM_152785.4 | 613 | Missense Mutation | CGT,TGT | R165C | NP_689998.1 |
XM_005247272.2 | 613 | Missense Mutation | CGT,TGT | R148C | XP_005247329.1 |
XM_011512627.2 | 613 | Missense Mutation | CGT,TGT | R168C | XP_011510929.1 |
XM_011512628.2 | 613 | Missense Mutation | CGT,TGT | R166C | XP_011510930.1 |
XM_011512629.1 | 613 | Missense Mutation | CGT,TGT | R149C | XP_011510931.1 |
XM_011512630.1 | 613 | Missense Mutation | CGT,TGT | R149C | XP_011510932.1 |