| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001163673.1 | 812 | Intron | NP_001157145.1 | ||
| NM_001163809.1 | 812 | Missense Mutation | CCG,CTG | P228L | NP_001157281.1 |
| NM_001163811.1 | 812 | Intron | NP_001157283.1 | ||
| NM_152348.3 | 812 | Intron | NP_689561.2 | ||
| XM_011523651.2 | 812 | Intron | XP_011521953.1 | ||
| XM_017024184.1 | 812 | Missense Mutation | CCG,CTG | P228L | XP_016879673.1 |