| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012338.3 | 714 | Missense Mutation | CCG,CTG | P278L | NP_036470.1 |
| XM_005250239.2 | 714 | Missense Mutation | CCG,CTG | P278L | XP_005250296.1 |
| XM_011515993.1 | 714 | Missense Mutation | CCG,CTG | P278L | XP_011514295.1 |
| XM_011515994.1 | 714 | Missense Mutation | CCG,CTG | P278L | XP_011514296.1 |
| XM_017011912.1 | 714 | Missense Mutation | CCG,CTG | P278L | XP_016867401.1 |
| XM_017011913.1 | 714 | Missense Mutation | CCG,CTG | P253L | XP_016867402.1 |
| XM_017011914.1 | 714 | Missense Mutation | CCG,CTG | P151L | XP_016867403.1 |