| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001080414.3 | 3270 | Missense Mutation | CCG,CTG | P2018L | NP_001073883.2 |
| XM_005267691.4 | 3270 | Intron | XP_005267748.1 | ||
| XM_011536796.2 | 3270 | Missense Mutation | CCG,CTG | P1982L | XP_011535098.1 |
| XM_017021335.1 | 3270 | Intron | XP_016876824.1 | ||
| XM_017021336.1 | 3270 | Missense Mutation | CCG,CTG | P1045L | XP_016876825.1 |
| XM_017021337.1 | 3270 | Intron | XP_016876826.1 |