| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017629.3 | 182 | Missense Mutation | CAG,CCG | Q36P | NP_060099.2 |
| XM_005270578.3 | 182 | UTR 5 | XP_005270635.1 | ||
| XM_005270579.3 | 182 | Intron | XP_005270636.1 | ||
| XM_011540883.2 | 182 | Intron | XP_011539185.1 | ||
| XM_011540884.2 | 182 | Intron | XP_011539186.1 | ||
| XM_017000529.1 | 182 | Missense Mutation | CAG,CCG | Q36P | XP_016856018.1 |