| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001143948.1 | 1022 | Missense Mutation | AAG,AGG | K245R | NP_001137420.1 |
| NM_032744.3 | 1022 | Missense Mutation | AAG,AGG | K227R | NP_116133.1 |
| XM_005249454.3 | 1022 | Missense Mutation | AAG,AGG | K227R | XP_005249511.1 |
| XM_011514956.1 | 1022 | UTR 3 | XP_011513258.1 | ||
| XM_011514958.2 | 1022 | Intron | XP_011513260.1 | ||
| XM_011514959.1 | 1022 | Intron | XP_011513261.1 | ||
| XM_017011377.1 | 1022 | UTR 3 | XP_016866866.1 |