| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318140.1 | 1573 | Missense Mutation | CGG,TGG | R22W | NP_001305069.1 |
| NM_001318141.1 | 1573 | Missense Mutation | CGG,TGG | R22W | NP_001305070.1 |
| NM_001318142.1 | 1573 | Intron | NP_001305071.1 | ||
| NM_001318143.1 | 1573 | Intron | NP_001305072.1 | ||
| NM_145312.3 | 1573 | Missense Mutation | CGG,TGG | R22W | NP_660355.2 |
| XM_011539498.2 | 1573 | UTR 5 | XP_011537800.1 |