| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001166034.1 | 1622 | Missense Mutation | AAT,AGT | N529S | NP_001159506.1 |
| NM_001166035.1 | 1622 | Intron | NP_001159507.1 | ||
| NM_198538.3 | 1622 | Missense Mutation | AAT,AGT | N186S | NP_940940.1 |
| XM_011526929.2 | 1622 | Missense Mutation | AAT,AGT | N511S | XP_011525231.1 |
| XM_011526930.2 | 1622 | Missense Mutation | AAT,AGT | N511S | XP_011525232.1 |
| XM_011526931.2 | 1622 | Missense Mutation | AAT,AGT | N493S | XP_011525233.1 |