| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199149.1 | 2125 | Missense Mutation | CCG,CTG | P603L | NP_001186078.1 |
| NM_001321121.1 | 2125 | Missense Mutation | CCG,CTG | P645L | NP_001308050.1 |
| NM_001321122.1 | 2125 | Missense Mutation | CCG,CTG | P634L | NP_001308051.1 |
| NM_002343.5 | 2125 | Missense Mutation | CCG,CTG | P647L | NP_002334.2 |