| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001270523.1 | 856 | Missense Mutation | CCG,CTG | P140L | NP_001257452.1 |
| NM_001270524.1 | 856 | Missense Mutation | CCG,CTG | P140L | NP_001257453.1 |
| NM_001270525.1 | 856 | Missense Mutation | CCG,CTG | P148L | NP_001257454.1 |
| NM_021728.3 | 856 | Missense Mutation | CCG,CTG | P148L | NP_068374.1 |
| NM_172337.2 | 856 | Missense Mutation | CCG,CTG | P140L | NP_758840.1 |