| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_007371.3 | 2635 | Missense Mutation | CCG,CTG | P699L | NP_031397.1 |
| XM_006717291.2 | 2635 | Missense Mutation | CCG,CTG | P699L | XP_006717354.1 |
| XM_011519052.2 | 2635 | Missense Mutation | CCG,CTG | P699L | XP_011517354.1 |
| XM_017015165.1 | 2635 | Missense Mutation | CCG,CTG | P698L | XP_016870654.1 |
| XM_017015166.1 | 2635 | Missense Mutation | CCG,CTG | P378L | XP_016870655.1 |