| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001039199.2 | 333 | Missense Mutation | CGG,CTG | R66L | NP_001034288.1 |
| NM_001261839.1 | 333 | Missense Mutation | CGG,CTG | R66L | NP_001248768.1 |
| NM_024331.4 | 333 | Missense Mutation | CGG,CTG | R66L | NP_077307.2 |
| XM_011529043.2 | 333 | Missense Mutation | CGG,CTG | R66L | XP_011527345.1 |
| XM_011529044.2 | 333 | Missense Mutation | CGG,CTG | R66L | XP_011527346.1 |
| XM_011529045.2 | 333 | Missense Mutation | CGG,CTG | R66L | XP_011527347.1 |
| XM_017028063.1 | 333 | Missense Mutation | CGG,CTG | R66L | XP_016883552.1 |