| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000701.7 | 1795 | Missense Mutation | ATC,GTC | I478V | NP_000692.2 |
| NM_001160233.1 | 1795 | Missense Mutation | ATC,GTC | I478V | NP_001153705.1 |
| NM_001160234.1 | 1795 | Missense Mutation | ATC,GTC | I447V | NP_001153706.1 |
| XM_017001360.1 | 1795 | Missense Mutation | ATC,GTC | I447V | XP_016856849.1 |
| XM_017001361.1 | 1795 | Missense Mutation | ATC,GTC | I447V | XP_016856850.1 |