| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001144033.1 | 937 | Missense Mutation | CCT,GCT | P230A | NP_001137505.1 |
| NM_145286.2 | 937 | Missense Mutation | CCT,GCT | P239A | NP_660329.1 |
| XM_017020400.1 | 937 | Missense Mutation | CCT,GCT | P168A | XP_016875889.1 |