| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271003.1 | 919 | Missense Mutation | CGG,TGG | R217W | NP_001257932.1 |
| NM_001271004.1 | 919 | UTR 3 | NP_001257933.1 | ||
| NM_006528.3 | 919 | Missense Mutation | CGG,TGG | R228W | NP_006519.1 |