| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001172668.1 | 1638 | Missense Mutation | CCA,TCA | P443S | NP_001166139.1 |
| NM_001172669.1 | 1638 | Missense Mutation | CCA,TCA | P466S | NP_001166140.1 |
| NM_001172670.1 | 1638 | Missense Mutation | CCA,TCA | P443S | NP_001166141.1 |
| NM_024706.4 | 1638 | Missense Mutation | CCA,TCA | P443S | NP_078982.3 |