| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142272.1 | 809 | Intron | NP_001135744.1 | ||
| NM_014700.3 | 809 | Missense Mutation | CCT,GCT | P142A | NP_055515.1 |
| XM_005255713.3 | 809 | Missense Mutation | CCT,GCT | P142A | XP_005255770.1 |
| XM_005255714.1 | 809 | Intron | XP_005255771.1 | ||
| XM_005255715.4 | 809 | Intron | XP_005255772.1 | ||
| XM_005255717.3 | 809 | Missense Mutation | CCT,GCT | P142A | XP_005255774.1 |
| XM_005255718.3 | 809 | Missense Mutation | CCT,GCT | P142A | XP_005255775.1 |
| XM_011522764.2 | 809 | Intron | XP_011521066.1 | ||
| XM_011522765.2 | 809 | Intron | XP_011521067.1 | ||
| XM_017023907.1 | 809 | Missense Mutation | CCT,GCT | P142A | XP_016879396.1 |