| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001159673.1 | 2168 | Intron | NP_001153145.1 | ||
| NM_001159674.1 | 2168 | Intron | NP_001153146.1 | ||
| NM_001159675.1 | 2168 | Silent Mutation | CAA,CAG | Q557Q | NP_001153147.1 |
| NM_001159676.1 | 2168 | Intron | NP_001153148.1 | ||
| NM_001159677.1 | 2168 | Intron | NP_001153149.1 | ||
| NM_001253771.1 | 2168 | Intron | NP_001240700.1 | ||
| NM_006372.4 | 2168 | Silent Mutation | CAA,CAG | Q592Q | NP_006363.4 |
| XM_005248635.4 | 2168 | Intron | XP_005248692.1 | ||
| XM_005248636.2 | 2168 | Silent Mutation | CAA,CAG | Q494Q | XP_005248693.1 |
| XM_005248637.2 | 2168 | Silent Mutation | CAA,CAG | Q592Q | XP_005248694.1 |
| XM_017010176.1 | 2168 | Silent Mutation | CAA,CAG | Q592Q | XP_016865665.1 |
| XM_017010177.1 | 2168 | Silent Mutation | CAA,CAG | Q592Q | XP_016865666.1 |
| XM_017010178.1 | 2168 | Intron | XP_016865667.1 | ||
| XM_017010179.1 | 2168 | Intron | XP_016865668.1 | ||
| XM_017010180.1 | 2168 | Intron | XP_016865669.1 |