| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001165977.2 | 424 | Missense Mutation | CGG,CTG | R101L | NP_001159449.1 |
| NM_001165978.2 | 424 | Missense Mutation | CGG,CTG | R101L | NP_001159450.1 |
| NM_001321070.1 | 424 | UTR 5 | NP_001307999.1 | ||
| NM_144707.3 | 424 | Missense Mutation | CGG,CTG | R101L | NP_653308.2 |
| XM_006712301.2 | 424 | Intron | XP_006712364.1 | ||
| XM_011510672.2 | 424 | Missense Mutation | CGG,CTG | R101L | XP_011508974.1 |