| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001301054.1 | 687 | Missense Mutation | ATT,GTT | I192V | NP_001287983.1 |
| NM_001301057.1 | 687 | Intron | NP_001287986.1 | ||
| NM_024028.3 | 687 | Missense Mutation | ATT,GTT | I209V | NP_076933.3 |
| XM_011537680.1 | 687 | Missense Mutation | ATT,GTT | I91V | XP_011535982.1 |
| XM_011537681.1 | 687 | Missense Mutation | ATT,GTT | I91V | XP_011535983.1 |
| XM_011537682.2 | 687 | UTR 5 | XP_011535984.1 |