| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_203373.2 | 13 | Missense Mutation | CAG,CTG | Q4L | NP_976307.2 |
| XM_005254320.3 | 13 | Missense Mutation | CAG,CTG | Q4L | XP_005254377.1 |
| XM_006720478.1 | 13 | Intron | XP_006720541.1 | ||
| XM_011521468.2 | 13 | UTR 5 | XP_011519770.1 | ||
| XM_011521469.1 | 13 | UTR 5 | XP_011519771.1 | ||
| XM_011521472.2 | 13 | UTR 5 | XP_011519774.1 | ||
| XM_017022086.1 | 13 | Missense Mutation | CAG,CTG | Q4L | XP_016877575.1 |