Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001289807.1 | 674 | Missense Mutation | CGG,TGG | R123W | NP_001276736.1 |
NM_001289808.1 | 674 | Missense Mutation | CGG,TGG | R123W | NP_001276737.1 |
NM_001885.2 | 674 | Missense Mutation | CGG,TGG | R123W | NP_001876.1 |
XM_011542608.1 | 674 | Missense Mutation | CGG,TGG | R123W | XP_011540910.1 |
XM_011542609.2 | 674 | Missense Mutation | CGG,TGG | R56W | XP_011540911.1 |