| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001171184.1 | 622 | Intron | NP_001164655.1 | ||
| NM_001939.2 | 622 | Missense Mutation | CAA,CGA | Q32R | NP_001930.2 |
| XM_017029333.1 | 622 | Missense Mutation | CAA,CGA | Q32R | XP_016884822.1 |
| XM_017029334.1 | 622 | UTR 5 | XP_016884823.1 |