| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282601.1 | 761 | Missense Mutation | CCT,TCT | P118S | NP_001269530.1 |
| NM_001282602.1 | 761 | Intron | NP_001269531.1 | ||
| NM_001282603.1 | 761 | Missense Mutation | CCT,TCT | P85S | NP_001269532.1 |
| NM_001282604.1 | 761 | Missense Mutation | CCT,TCT | P122S | NP_001269533.1 |
| NM_001282605.1 | 761 | Intron | NP_001269534.1 | ||
| NM_006601.6 | 761 | Missense Mutation | CCT,TCT | P118S | NP_006592.3 |
| XM_005268576.4 | 761 | Missense Mutation | CCT,TCT | P122S | XP_005268633.1 |
| XM_006719199.2 | 761 | Intron | XP_006719262.1 | ||
| XM_011537773.2 | 761 | Intron | XP_011536075.1 | ||
| XM_011537774.2 | 761 | Missense Mutation | CCT,TCT | P122S | XP_011536076.1 |
| XM_017018716.1 | 761 | Missense Mutation | CCT,TCT | P122S | XP_016874205.1 |