| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001030055.1 | 2188 | Missense Mutation | CAG,CGG | Q635R | NP_001025226.1 |
| NM_001173.2 | 2188 | Missense Mutation | CAG,CGG | Q635R | NP_001164.2 |
| XM_005267635.3 | 2188 | Missense Mutation | CAG,CGG | Q635R | XP_005267692.1 |
| XM_005267636.3 | 2188 | Missense Mutation | CAG,CGG | Q635R | XP_005267693.1 |
| XM_017021287.1 | 2188 | Missense Mutation | CAG,CGG | Q635R | XP_016876776.1 |
| XM_017021288.1 | 2188 | Missense Mutation | CAG,CGG | Q635R | XP_016876777.1 |