| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001122979.2 | 1714 | Silent Mutation | CTA,CTG | L234L | NP_001116451.1 |
| NM_001170631.1 | 1714 | Missense Mutation | ACC,GCC | T502A | NP_001164102.1 |
| NM_032029.4 | 1714 | Silent Mutation | CTA,CTG | L234L | NP_114418.2 |
| XM_011510051.2 | 1714 | Missense Mutation | ACC,GCC | T502A | XP_011508353.1 |
| XM_011510052.2 | 1714 | Missense Mutation | ACC,GCC | T490A | XP_011508354.1 |
| XM_017002442.1 | 1714 | Missense Mutation | ACC,GCC | T502A | XP_016857931.1 |