| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282788.1 | 280 | Missense Mutation | CCG,CTG | P46L | NP_001269717.1 |
| NM_001282789.1 | 280 | Intron | NP_001269718.1 | ||
| NM_032599.3 | 280 | Missense Mutation | CCG,CTG | P46L | NP_115988.1 |
| XM_017012743.1 | 280 | Missense Mutation | CCG,CTG | P46L | XP_016868232.1 |