Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001038603.2 | 277 | Missense Mutation | CGG,TGG | R39W | NP_001033692.2 |
NM_001244734.1 | 277 | Missense Mutation | CGG,TGG | R39W | NP_001231663.1 |
XM_005248445.4 | 277 | Missense Mutation | CGG,TGG | R39W | XP_005248502.1 |
XM_005248446.4 | 277 | Missense Mutation | CGG,TGG | R39W | XP_005248503.1 |
XM_005248447.4 | 277 | Missense Mutation | CGG,TGG | R39W | XP_005248504.1 |