Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271895.1 | 636 | Missense Mutation | CGG,TGG | R196W | NP_001258824.1 |
NM_001271896.1 | 636 | Missense Mutation | CGG,TGG | R196W | NP_001258825.1 |
NM_025150.4 | 636 | Missense Mutation | CGG,TGG | R196W | NP_079426.2 |
XM_006711555.1 | 636 | Missense Mutation | CGG,TGG | R196W | XP_006711618.1 |
XM_006711556.1 | 636 | Missense Mutation | CGG,TGG | R196W | XP_006711619.1 |
XM_017002394.1 | 636 | Missense Mutation | CGG,TGG | R196W | XP_016857883.1 |
XM_017002395.1 | 636 | Missense Mutation | CGG,TGG | R196W | XP_016857884.1 |