| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001297655.1 | 506 | Missense Mutation | CGG,TGG | R93W | NP_001284584.1 |
| NM_001297656.1 | 506 | Missense Mutation | CGG,TGG | R39W | NP_001284585.1 |
| NM_001297657.1 | 506 | UTR 5 | NP_001284586.1 | ||
| NM_006845.3 | 506 | Missense Mutation | CGG,TGG | R93W | NP_006836.2 |
| XM_011540540.2 | 506 | UTR 5 | XP_011538842.1 | ||
| XM_011540541.2 | 506 | UTR 5 | XP_011538843.1 |