| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001164269.1 | 372 | Silent Mutation | ACA,ACG | T76T | NP_001157741.1 |
| NM_001164270.1 | 372 | Intron | NP_001157742.1 | ||
| NM_002875.4 | 372 | Intron | NP_002866.2 | ||
| NM_133487.3 | 372 | Silent Mutation | ACA,ACG | T76T | NP_597994.3 |
| XM_006720626.3 | 372 | Intron | XP_006720689.1 | ||
| XM_011521857.2 | 372 | Intron | XP_011520159.1 | ||
| XM_011521858.2 | 372 | Intron | XP_011520160.1 | ||
| XM_011521859.2 | 372 | Intron | XP_011520161.1 | ||
| XM_011521860.2 | 372 | Intron | XP_011520162.1 | ||
| XM_011521861.2 | 372 | Intron | XP_011520163.1 | ||
| XM_011521862.2 | 372 | Intron | XP_011520164.1 |