| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_013320.2 | 458 | Missense Mutation | CCT,TCT | P119S | NP_037452.1 |
| XM_017019241.1 | 458 | Missense Mutation | CCT,TCT | P119S | XP_016874730.1 |
| XM_017019242.1 | 458 | Missense Mutation | CCT,TCT | P119S | XP_016874731.1 |