| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001287497.1 | 2137 | Missense Mutation | CCG,CTG | P582L | NP_001274426.1 |
| NM_022484.5 | 2137 | Missense Mutation | CCG,CTG | P582L | NP_071929.3 |
| XM_017012523.1 | 2137 | Missense Mutation | CCG,CTG | P582L | XP_016868012.1 |
| XM_017012524.1 | 2137 | Intron | XP_016868013.1 | ||
| XM_017012525.1 | 2137 | Missense Mutation | CCG,CTG | P198L | XP_016868014.1 |