| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001143763.1 | 982 | Missense Mutation | GCC,TCC | A293S | NP_001137235.1 |
| NM_001143764.1 | 982 | Missense Mutation | GCC,TCC | A293S | NP_001137236.1 |
| NM_130784.2 | 982 | Missense Mutation | GCC,TCC | A257S | NP_570140.1 |