| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001301144.1 | 362 | Intron | NP_001288073.1 | ||
| NM_001301145.1 | 362 | Intron | NP_001288074.1 | ||
| NM_001301146.1 | 362 | Intron | NP_001288075.1 | ||
| NM_080745.4 | 362 | Intron | NP_542783.2 | ||
| NM_182985.4 | 362 | Missense Mutation | CCC,GCC | P7A | NP_892030.3 |