| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001177996.1 | 569 | Missense Mutation | ATC,GTC | I73V | NP_001171467.1 |
| NM_001177997.1 | 569 | Missense Mutation | ATC,GTC | I60V | NP_001171468.1 |
| NM_144671.4 | 569 | Missense Mutation | ATC,GTC | I60V | NP_653272.2 |
| XM_006719257.3 | 569 | Missense Mutation | ATC,GTC | I60V | XP_006719320.1 |
| XM_011537976.2 | 569 | Missense Mutation | ATC,GTC | I60V | XP_011536278.1 |
| XM_017018883.1 | 569 | Missense Mutation | ATC,GTC | I60V | XP_016874372.1 |