| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_173615.4 | 601 | Missense Mutation | CAG,CTG | Q112L | NP_775886.3 |
| XM_011545742.2 | 601 | Missense Mutation | CAG,CTG | Q112L | XP_011544044.1 |
| XM_011545744.2 | 601 | Intron | XP_011544046.1 | ||
| XM_011545745.1 | 601 | Intron | XP_011544047.1 | ||
| XM_011545746.2 | 601 | Intron | XP_011544048.1 | ||
| XM_017022947.1 | 601 | Missense Mutation | CAG,CTG | Q112L | XP_016878436.1 |
| XM_017022948.1 | 601 | Intron | XP_016878437.1 | ||
| XM_017022949.1 | 601 | Intron | XP_016878438.1 |