| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001290261.1 | 1901 | Missense Mutation | CAG,CGG | Q677R | NP_001277190.1 |
| NM_015655.3 | 1901 | Missense Mutation | CAG,CGG | Q677R | NP_056470.1 |
| XM_005260702.3 | 1901 | Missense Mutation | CAG,CGG | Q645R | XP_005260759.1 |
| XM_006723558.3 | 1901 | Missense Mutation | CAG,CGG | Q677R | XP_006723621.1 |
| XM_011529219.2 | 1901 | Missense Mutation | CAG,CGG | Q677R | XP_011527521.1 |
| XM_017027802.1 | 1901 | Missense Mutation | CAG,CGG | Q645R | XP_016883291.1 |
| XM_017027803.1 | 1901 | Missense Mutation | CAG,CGG | Q645R | XP_016883292.1 |
| XM_017027804.1 | 1901 | Missense Mutation | CAG,CGG | Q612R | XP_016883293.1 |