| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000413.2 | 699 | Missense Mutation | CGT,GGT | R22G | NP_000404.2 |
| XM_005257292.3 | 699 | Missense Mutation | CGT,GGT | R22G | XP_005257349.1 |
| XM_006721857.3 | 699 | Missense Mutation | CGT,GGT | R22G | XP_006721920.1 |
| XM_006721858.3 | 699 | Missense Mutation | CGT,GGT | R22G | XP_006721921.1 |
| XM_006721859.3 | 699 | Missense Mutation | CGT,GGT | R22G | XP_006721922.1 |
| XM_011524729.1 | 699 | Missense Mutation | CGT,GGT | R22G | XP_011523031.1 |
| XM_011524730.1 | 699 | Missense Mutation | CGT,GGT | R22G | XP_011523032.1 |
| XM_011524731.1 | 699 | Missense Mutation | CGT,GGT | R22G | XP_011523033.1 |
| XM_011524732.2 | 699 | Missense Mutation | CGT,GGT | R22G | XP_011523034.1 |