| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_022117.3 | 656 | Missense Mutation | CCG,TCG | P162S | NP_071400.1 |
| XM_006724592.3 | 656 | Missense Mutation | CCG,TCG | P162S | XP_006724655.1 |
| XM_017029726.1 | 656 | Missense Mutation | CCG,TCG | P162S | XP_016885215.1 |
| XM_017029727.1 | 656 | Missense Mutation | CCG,TCG | P162S | XP_016885216.1 |