| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001302770.1 | 362 | Missense Mutation | CCT,TCT | P115S | NP_001289699.1 |
| NM_001891.3 | 362 | Missense Mutation | CCT,TCT | P116S | NP_001882.1 |
| XM_017007760.1 | 362 | Missense Mutation | CCT,TCT | P116S | XP_016863249.1 |