Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_199285.2 | 292 | Missense Mutation | CGG,TGG | R68W | NP_954979.2 |
XM_005258779.4 | 292 | Missense Mutation | CGG,TGG | R120W | XP_005258836.2 |
XM_005258780.3 | 292 | Missense Mutation | CGG,TGG | R68W | XP_005258837.1 |
XM_006723154.3 | 292 | Missense Mutation | CGG,TGG | R68W | XP_006723217.1 |
XM_011526787.1 | 292 | Missense Mutation | CGG,TGG | R68W | XP_011525089.1 |
XM_011526788.1 | 292 | Missense Mutation | CGG,TGG | R68W | XP_011525090.1 |
XM_011526789.2 | 292 | Missense Mutation | CGG,TGG | R68W | XP_011525091.1 |
XM_011526790.2 | 292 | Missense Mutation | CGG,TGG | R68W | XP_011525092.1 |