| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001297713.1 | 2719 | Missense Mutation | CCG,TCG | P561S | NP_001284642.1 |
| NM_015441.2 | 2719 | Missense Mutation | CCG,TCG | P560S | NP_056256.1 |
| XM_005245075.2 | 2719 | Missense Mutation | CCG,TCG | P562S | XP_005245132.1 |
| XM_011509398.2 | 2719 | Missense Mutation | CCG,TCG | P320S | XP_011507700.1 |
| XM_017000967.1 | 2719 | Intron | XP_016856456.1 |