| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001185063.2 | 2351 | Intron | NP_001171992.1 | ||
| NM_007131.4 | 2351 | Silent Mutation | GCA,GCC | A140A | NP_009062.2 |
| XM_005262469.1 | 2351 | Silent Mutation | GCA,GCC | A140A | XP_005262526.1 |
| XM_005262471.3 | 2351 | UTR 5 | XP_005262528.1 | ||
| XM_011531391.1 | 2351 | Silent Mutation | GCA,GCC | A140A | XP_011529693.1 |
| XM_011531395.2 | 2351 | Missense Mutation | CAC,CCC | H21P | XP_011529697.1 |
| XM_011531396.2 | 2351 | UTR 5 | XP_011529698.1 | ||
| XM_011531397.2 | 2351 | UTR 5 | XP_011529699.1 | ||
| XM_017029818.1 | 2351 | Missense Mutation | CAC,CCC | H25P | XP_016885307.1 |
| XM_017029819.1 | 2351 | Missense Mutation | CAC,CCC | H37P | XP_016885308.1 |
| XM_017029820.1 | 2351 | UTR 5 | XP_016885309.1 |