| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001311182.1 | 741 | Missense Mutation | TCC,TTC | S186F | NP_001298111.1 |
| NM_022046.5 | 741 | Missense Mutation | TCC,TTC | S186F | NP_071329.2 |
| XM_017026820.1 | 741 | UTR 3 | XP_016882309.1 |