| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014246.1 | 5571 | Missense Mutation | CCT,GCT | P2983A | NP_055061.1 |
| XM_006724383.3 | 5571 | Missense Mutation | CCT,GCT | P2983A | XP_006724446.1 |
| XM_011530553.1 | 5571 | Intron | XP_011528855.1 | ||
| XM_011530554.2 | 5571 | Missense Mutation | CCT,GCT | P1814A | XP_011528856.1 |
| XM_011530555.2 | 5571 | Missense Mutation | CCT,GCT | P1782A | XP_011528857.1 |