| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001323369.1 | 468 | Silent Mutation | TGC,TGT | C91C | NP_001310298.1 |
| NM_001323370.1 | 468 | Silent Mutation | TGC,TGT | C91C | NP_001310299.1 |
| NM_003881.3 | 468 | Silent Mutation | TGC,TGT | C91C | NP_003872.1 |
| XM_017028116.1 | 468 | UTR 5 | XP_016883605.1 | ||
| XM_017028117.1 | 468 | Silent Mutation | TGC,TGT | C149C | XP_016883606.1 |