| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001038633.3 | 1398 | Missense Mutation | CAG,CGG | Q169R | NP_001033722.1 |
| NM_001242908.1 | 1398 | Missense Mutation | CAG,CGG | Q169R | NP_001229837.1 |
| NM_001242909.1 | 1398 | Missense Mutation | CAG,CGG | Q142R | NP_001229838.1 |
| NM_001242910.1 | 1398 | Intron | NP_001229839.1 | ||
| XM_006710583.3 | 1398 | Missense Mutation | CAG,CGG | Q169R | XP_006710646.1 |