| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| XM_005268208.1 | 2632 | Silent Mutation | ACG,ACT | T898T | XP_005268265.1 |
| XM_005268209.3 | 2632 | Silent Mutation | ACG,ACT | T780T | XP_005268266.1 |
| XM_017021765.1 | 2632 | Silent Mutation | ACG,ACT | T768T | XP_016877254.1 |