| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286389.1 | 466 | Silent Mutation | TGC,TGT | C149C | NP_001273318.1 |
| NM_001286390.1 | 466 | Silent Mutation | TGC,TGT | C149C | NP_001273319.1 |
| XM_011536745.2 | 466 | Silent Mutation | TGC,TGT | C103C | XP_011535047.1 |
| XM_011536746.2 | 466 | Intron | XP_011535048.1 | ||
| XM_011536750.2 | 466 | Silent Mutation | TGC,TGT | C50C | XP_011535052.1 |