| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001033504.1 | 608 | Missense Mutation | CCC,GCC | P76A | NP_001028676.1 |
| NM_001301746.1 | 608 | Missense Mutation | CCC,GCC | P76A | NP_001288675.1 |
| NM_015544.2 | 608 | Missense Mutation | CCC,GCC | P76A | NP_056359.2 |