| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001303279.1 | 3287 | Intron | NP_001290208.1 | ||
| NM_001303280.1 | 3287 | Intron | NP_001290209.1 | ||
| NM_015194.2 | 3287 | Missense Mutation | CGC,TGC | R996C | NP_056009.1 |
| XM_017024685.1 | 3287 | Intron | XP_016880174.1 |