| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321190.1 | 642 | Silent Mutation | TGC,TGT | C2C | NP_001308119.1 |
| NM_001321191.1 | 642 | Intron | NP_001308120.1 | ||
| NM_006666.2 | 642 | Intron | NP_006657.1 | ||
| XM_011526330.1 | 642 | Intron | XP_011524632.1 |