| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001002838.3 | 5520 | Missense Mutation | CCG,CTG | P1637L | NP_001002838.1 |
| NM_020922.4 | 5520 | Missense Mutation | CCG,CTG | P1694L | NP_065973.2 |
| XM_006724593.3 | 5520 | Missense Mutation | CCG,CTG | P1637L | XP_006724656.1 |
| XM_011530802.2 | 5520 | Missense Mutation | CCG,CTG | P1647L | XP_011529104.1 |
| XM_017029741.1 | 5520 | Missense Mutation | CCG,CTG | P1694L | XP_016885230.1 |
| XM_017029742.1 | 5520 | Missense Mutation | CCG,CTG | P1694L | XP_016885231.1 |
| XM_017029743.1 | 5520 | Missense Mutation | CCG,CTG | P1694L | XP_016885232.1 |
| XM_017029744.1 | 5520 | Missense Mutation | CCG,CTG | P1694L | XP_016885233.1 |
| XM_017029745.1 | 5520 | Missense Mutation | CCG,CTG | P1684L | XP_016885234.1 |