| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001280796.1 | 1851 | Missense Mutation | CAG,CTG | Q286L | NP_001267725.1 |
| NM_001280797.1 | 1851 | Missense Mutation | CAG,CTG | Q297L | NP_001267726.1 |
| NM_001280798.1 | 1851 | Missense Mutation | CAG,CTG | Q297L | NP_001267727.1 |
| NM_013267.3 | 1851 | Missense Mutation | CAG,CTG | Q562L | NP_037399.2 |
| XM_005268797.1 | 1851 | Missense Mutation | CAG,CTG | Q526L | XP_005268854.1 |
| XM_017019180.1 | 1851 | Missense Mutation | CAG,CTG | Q297L | XP_016874669.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_207344.3 | 1851 | Intron | NP_997227.1 |