Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001012267.2 | 1622 | Intron | NP_001012267.1 | ||
NM_001286969.1 | 1622 | Intron | NP_001273898.1 | ||
NM_001286971.1 | 1622 | Intron | NP_001273900.1 | ||
XM_011518685.2 | 1622 | Intron | XP_011516987.1 | ||
XM_011518689.1 | 1622 | Intron | XP_011516991.1 | ||
XM_017014715.1 | 1622 | Intron | XP_016870204.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_022755.5 | 1622 | Missense Mutation | CCC,TCC | P449S | NP_073592.1 |
XM_017015041.1 | 1622 | UTR 3 | XP_016870530.1 |