| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000543.4 | 381 | Missense Mutation | CCC,TCC | P66S | NP_000534.3 |
| NM_001007593.2 | 381 | Missense Mutation | CCC,TCC | P66S | NP_001007594.2 |
| NM_001318087.1 | 381 | Missense Mutation | CCC,TCC | P66S | NP_001305016.1 |
| NM_001318088.1 | 381 | UTR 5 | NP_001305017.1 | ||
| XM_011520303.1 | 381 | Missense Mutation | CCC,TCC | P66S | XP_011518605.1 |
| XM_011520304.1 | 381 | Missense Mutation | CCC,TCC | P66S | XP_011518606.1 |