| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001244638.1 | 478 | Intron | NP_001231567.1 | ||
| NM_032199.2 | 478 | Missense Mutation | CGG,TGG | R8W | NP_115575.1 |
| XM_011540262.1 | 478 | Missense Mutation | CGG,TGG | R8W | XP_011538564.1 |
| XM_017016765.1 | 478 | Intron | XP_016872254.1 |