| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001111298.2 | 926 | Silent Mutation | TGC,TGT | C327C | NP_001104768.2 |
| NM_001286360.1 | 926 | Silent Mutation | TGC,TGT | C269C | NP_001273289.1 |
| NM_001286361.1 | 926 | UTR 3 | NP_001273290.1 | ||
| NM_173672.4 | 926 | Silent Mutation | TGC,TGT | C301C | NP_775943.1 |
| XM_011535765.2 | 926 | Silent Mutation | TGC,TGT | C295C | XP_011534067.1 |
| XM_011535766.2 | 926 | Intron | XP_011534068.1 | ||
| XM_011535767.2 | 926 | Intron | XP_011534069.1 | ||
| XM_011535769.2 | 926 | Intron | XP_011534071.1 | ||
| XM_017010774.1 | 926 | UTR 3 | XP_016866263.1 |