| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282237.1 | 2371 | Missense Mutation | CCG,TCG | P696S | NP_001269166.1 |
| NM_001282238.1 | 2371 | Missense Mutation | CCG,TCG | P625S | NP_001269167.1 |
| NM_022898.2 | 2371 | Missense Mutation | CCG,TCG | P626S | NP_075049.1 |
| NM_138576.3 | 2371 | Missense Mutation | CCG,TCG | P697S | NP_612808.1 |