Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000022.3 | 908 | Missense Mutation | CGG,TGG | R253W | NP_000013.2 |
NM_001322050.1 | 908 | Missense Mutation | CGG,TGG | R118W | NP_001308979.1 |
NM_001322051.1 | 908 | Missense Mutation | CGG,TGG | R229W | NP_001308980.1 |