| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001170722.1 | 195 | Missense Mutation | CCG,CTG | P36L | NP_001164193.1 |
| NM_001170723.1 | 195 | Missense Mutation | CCG,CTG | P28L | NP_001164194.1 |
| NM_001170724.1 | 195 | Missense Mutation | CCG,CTG | P28L | NP_001164195.1 |
| NM_032126.4 | 195 | Missense Mutation | CCG,CTG | P28L | NP_115502.2 |