| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001135058.1 | 314 | Missense Mutation | CCG,CTG | P19L | NP_001128530.1 |
| NM_004086.2 | 314 | Missense Mutation | CCG,CTG | P19L | NP_004077.1 |
| XM_017021071.1 | 314 | Missense Mutation | CCG,CTG | P19L | XP_016876560.1 |
| XM_017021072.1 | 314 | Missense Mutation | CCG,CTG | P19L | XP_016876561.1 |
| XM_017021073.1 | 314 | Intron | XP_016876562.1 |