| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130725.1 | 762 | Missense Mutation | CCT,CTT | P65L | NP_001124197.1 |
| NM_001144932.2 | 762 | Missense Mutation | CCT,CTT | P168L | NP_001138404.1 |
| NM_002797.4 | 762 | Missense Mutation | CCT,CTT | P168L | NP_002788.1 |
| XM_005267871.2 | 762 | Missense Mutation | CCT,CTT | P168L | XP_005267928.1 |