| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001101404.1 | 46 | Missense Mutation | CGG,GGG | R16G | NP_001094874.1 |
| XM_011521895.2 | 46 | Missense Mutation | CGG,GGG | R16G | XP_011520197.1 |
| XM_011521896.2 | 46 | Intron | XP_011520198.1 | ||
| XM_011521899.2 | 46 | Intron | XP_011520201.1 | ||
| XM_017022487.1 | 46 | Intron | XP_016877976.1 | ||
| XM_017022488.1 | 46 | Intron | XP_016877977.1 |