| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304802.1 | 1489 | Missense Mutation | GGC,GTC | G376V | NP_001291731.1 |
| NM_001323894.1 | 1489 | Missense Mutation | GGC,GTC | G376V | NP_001310823.1 |
| NM_001323895.1 | 1489 | Missense Mutation | GGC,GTC | G247V | NP_001310824.1 |
| NM_001323896.1 | 1489 | Missense Mutation | GGC,GTC | G402V | NP_001310825.1 |
| NM_001323897.1 | 1489 | Missense Mutation | GGC,GTC | G402V | NP_001310826.1 |
| NM_018145.2 | 1489 | Missense Mutation | GGC,GTC | G376V | NP_060615.1 |
| XM_011521755.2 | 1489 | Missense Mutation | GGC,GTC | G170V | XP_011520057.1 |