| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256371.1 | 2596 | Missense Mutation | GCT,TCT | A692S | NP_001243300.1 |
| NM_001256372.1 | 2596 | Missense Mutation | GCT,TCT | A692S | NP_001243301.1 |
| NM_024680.3 | 2596 | Missense Mutation | GCT,TCT | A692S | NP_078956.2 |
| XM_011520367.1 | 2596 | Missense Mutation | GCT,TCT | A587S | XP_011518669.1 |