| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001297624.1 | 481 | Missense Mutation | CGG,CTG | R2L | NP_001284553.1 |
| NM_001297625.1 | 481 | UTR 5 | NP_001284554.1 | ||
| NM_144684.3 | 481 | Missense Mutation | CGG,CTG | R2L | NP_653285.2 |
| XM_011526465.2 | 481 | Missense Mutation | CGG,CTG | R2L | XP_011524767.1 |