| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001261464.1 | 234 | Missense Mutation | CCG,CTG | P50L | NP_001248393.1 |
| NM_001261465.1 | 234 | Missense Mutation | CCG,CTG | P40L | NP_001248394.1 |
| NM_001261466.1 | 234 | Nonsense Mutation | CGA,TGA | R50* | NP_001248395.1 |
| NM_003815.4 | 234 | Missense Mutation | CCG,CTG | P40L | NP_003806.3 |
| NM_207191.2 | 234 | Missense Mutation | CCG,CTG | P40L | NP_997074.1 |
| NM_207194.2 | 234 | Missense Mutation | CCG,CTG | P40L | NP_997077.1 |
| NM_207195.2 | 234 | Missense Mutation | CCG,CTG | P40L | NP_997078.1 |
| NM_207196.2 | 234 | Missense Mutation | CCG,CTG | P40L | NP_997079.1 |
| NM_207197.2 | 234 | Missense Mutation | CCG,CTG | P40L | NP_997080.1 |