| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001252100.1 | 3947 | Missense Mutation | CCT,TCT | P1616S | NP_001239029.1 |
| NM_001252102.1 | 3947 | Intron | NP_001239031.1 | ||
| NM_001252103.1 | 3947 | Intron | NP_001239032.1 | ||
| NM_017596.3 | 3947 | Missense Mutation | CCT,TCT | P1603S | NP_060066.2 |
| XM_017000731.1 | 3947 | Missense Mutation | CCT,TCT | P1560S | XP_016856220.1 |
| XM_017000732.1 | 3947 | Missense Mutation | CCT,TCT | P1215S | XP_016856221.1 |