| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_199242.2 | 3062 | Missense Mutation | CCT,GCT | P995A | NP_954712.1 |
| XM_011524504.1 | 3062 | Missense Mutation | CCT,GCT | P1018A | XP_011522806.1 |
| XM_011524506.1 | 3062 | Missense Mutation | CCT,GCT | P1017A | XP_011522808.1 |
| XM_011524507.2 | 3062 | Missense Mutation | CCT,GCT | P815A | XP_011522809.1 |