| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001184.3 | 7197 | Missense Mutation | CCT,GCT | P2434A | NP_001175.2 |
| XM_011512924.1 | 7197 | Missense Mutation | CCT,GCT | P2436A | XP_011511226.1 |
| XM_011512925.1 | 7197 | Missense Mutation | CCT,GCT | P2372A | XP_011511227.1 |
| XM_011512926.2 | 7197 | Intron | XP_011511228.1 | ||
| XM_017006643.1 | 7197 | Missense Mutation | CCT,GCT | P2370A | XP_016862132.1 |