| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_030636.2 | 1368 | Missense Mutation | CCT,CTT | P217L | NP_085139.2 |
| XM_017012657.1 | 1368 | Missense Mutation | CCT,CTT | P217L | XP_016868146.1 |
| XM_017012658.1 | 1368 | Missense Mutation | CCT,CTT | P217L | XP_016868147.1 |