| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001085354.2 | 2932 | Missense Mutation | CAT,CGT | H886R | NP_001078823.1 |
| NM_024657.4 | 2932 | Missense Mutation | ATC,GTC | I899V | NP_078933.3 |
| XM_005262190.3 | 2932 | Missense Mutation | ATC,GTC | I807V | XP_005262247.1 |
| XM_006724691.2 | 2932 | Missense Mutation | ATC,GTC | I777V | XP_006724754.1 |
| XM_011531027.2 | 2932 | Missense Mutation | ATC,GTC | I722V | XP_011529329.1 |
| XM_017029844.1 | 2932 | Missense Mutation | CAT,CGT | H794R | XP_016885333.1 |