| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001326559.1 | 1077 | Missense Mutation | CCG,CTG | P226L | NP_001313488.1 |
| NM_005070.3 | 1077 | Intron | NP_005061.2 | ||
| NM_201574.2 | 1077 | Missense Mutation | CCG,CTG | P226L | NP_963868.2 |
| XM_005246789.4 | 1077 | Missense Mutation | CCG,CTG | P226L | XP_005246846.1 |
| XM_005246790.4 | 1077 | Intron | XP_005246847.1 | ||
| XM_011511665.2 | 1077 | Missense Mutation | CCG,CTG | P173L | XP_011509967.1 |
| XM_011511667.2 | 1077 | Intron | XP_011509969.1 |