| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_018266.2 | 1512 | Missense Mutation | CAA,CGA | Q416R | NP_060736.1 |
| XM_005247578.1 | 1512 | Missense Mutation | AAC,GAC | N376D | XP_005247635.1 |
| XM_006713687.1 | 1512 | Missense Mutation | CAA,CGA | Q416R | XP_006713750.1 |
| XM_011512958.2 | 1512 | Intron | XP_011511260.1 | ||
| XM_017006788.1 | 1512 | Missense Mutation | CAA,CGA | Q388R | XP_016862277.1 |