| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_007342.2 | 626 | Missense Mutation | CAG,CGG | Q36R | NP_031368.1 |
| XM_005249592.1 | 626 | Missense Mutation | CAG,CGG | Q36R | XP_005249649.1 |
| XM_005249593.3 | 626 | UTR 5 | XP_005249650.1 | ||
| XM_011515104.2 | 626 | UTR 5 | XP_011513406.1 | ||
| XM_017011714.1 | 626 | UTR 5 | XP_016867203.1 | ||
| XM_017011715.1 | 626 | UTR 5 | XP_016867204.1 | ||
| XM_017011716.1 | 626 | UTR 5 | XP_016867205.1 | ||
| XM_017011717.1 | 626 | UTR 5 | XP_016867206.1 | ||
| XM_017011718.1 | 626 | Intron | XP_016867207.1 |