| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001290261.1 | 1771 | Missense Mutation | CGG,GGG | R634G | NP_001277190.1 |
| NM_015655.3 | 1771 | Missense Mutation | CGG,GGG | R634G | NP_056470.1 |
| XM_005260702.3 | 1771 | Missense Mutation | CGG,GGG | R602G | XP_005260759.1 |
| XM_006723558.3 | 1771 | Missense Mutation | CGG,GGG | R634G | XP_006723621.1 |
| XM_011529219.2 | 1771 | Missense Mutation | CGG,GGG | R634G | XP_011527521.1 |
| XM_017027802.1 | 1771 | Missense Mutation | CGG,GGG | R602G | XP_016883291.1 |
| XM_017027803.1 | 1771 | Missense Mutation | CGG,GGG | R602G | XP_016883292.1 |
| XM_017027804.1 | 1771 | Missense Mutation | CGG,GGG | R569G | XP_016883293.1 |