| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282933.1 | 383 | Missense Mutation | CCC,TCC | P41S | NP_001269862.1 |
| NM_001282935.1 | 383 | Silent Mutation | CGC,CGT | R16R | NP_001269864.1 |
| NM_032819.4 | 383 | Missense Mutation | CCC,TCC | P41S | NP_116208.3 |