| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001008779.1 | 333 | Missense Mutation | CGG,TGG | R43W | NP_001008779.1 |
| NM_001142634.1 | 333 | Missense Mutation | CGG,TGG | R43W | NP_001136106.1 |
| NM_182756.3 | 333 | Missense Mutation | CGG,TGG | R43W | NP_877433.2 |