| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001243224.1 | 607 | Missense Mutation | CGG,CTG | R25L | NP_001230153.1 |
| NM_004584.2 | 607 | Missense Mutation | CGG,CTG | R101L | NP_004575.1 |
| XM_006718652.3 | 607 | Missense Mutation | CGG,CTG | R112L | XP_006718715.1 |
| XM_017018097.1 | 607 | UTR 5 | XP_016873586.1 | ||
| XM_017018098.1 | 607 | UTR 5 | XP_016873587.1 |