| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286531.1 | 406 | Missense Mutation | GCT,GTT | A75V | NP_001273460.1 |
| NM_001286532.1 | 406 | Missense Mutation | GCT,GTT | A75V | NP_001273461.1 |
| NM_001286533.1 | 406 | UTR 5 | NP_001273462.1 | ||
| NM_001286534.1 | 406 | UTR 5 | NP_001273463.1 | ||
| NM_001286535.1 | 406 | Missense Mutation | GCT,GTT | A147V | NP_001273464.1 |
| NM_001286536.1 | 406 | Intron | NP_001273465.1 | ||
| NM_152442.3 | 406 | Missense Mutation | GCT,GTT | A147V | NP_689655.3 |
| XM_005253849.4 | 406 | Intron | XP_005253906.1 | ||
| XM_011537971.2 | 406 | Missense Mutation | GCT,GTT | A147V | XP_011536273.1 |
| XM_011537972.2 | 406 | Missense Mutation | GCT,GTT | A123V | XP_011536274.1 |
| XM_011537974.2 | 406 | Missense Mutation | GCT,GTT | A75V | XP_011536276.1 |
| XM_017018877.1 | 406 | Missense Mutation | GCT,GTT | A95V | XP_016874366.1 |
| XM_017018878.1 | 406 | Missense Mutation | GCT,GTT | A75V | XP_016874367.1 |
| XM_017018879.1 | 406 | Intron | XP_016874368.1 | ||
| XM_017018880.1 | 406 | Intron | XP_016874369.1 | ||
| XM_017018881.1 | 406 | Intron | XP_016874370.1 | ||
| XM_017018882.1 | 406 | UTR 5 | XP_016874371.1 |