| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256678.1 | 761 | Missense Mutation | CCT,CTT | P127L | NP_001243607.1 |
| NM_001256679.1 | 761 | Missense Mutation | CCT,CTT | P32L | NP_001243608.1 |
| NM_001256680.1 | 761 | Intron | NP_001243609.1 | ||
| NM_001256681.1 | 761 | Intron | NP_001243610.1 | ||
| NM_014672.3 | 761 | Missense Mutation | CCT,CTT | P127L | NP_055487.2 |
| XM_005268237.3 | 761 | Missense Mutation | CCT,CTT | P127L | XP_005268294.1 |
| XM_011537409.2 | 761 | Missense Mutation | CCT,CTT | P127L | XP_011535711.1 |
| XM_011537410.2 | 761 | Missense Mutation | CCT,CTT | P127L | XP_011535712.1 |
| XM_017021835.1 | 761 | Missense Mutation | CCT,CTT | P127L | XP_016877324.1 |
| XM_017021836.1 | 761 | Missense Mutation | CCT,CTT | P127L | XP_016877325.1 |
| XM_017021837.1 | 761 | Missense Mutation | CCT,CTT | P127L | XP_016877326.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001305155.1 | 761 | Intron | NP_001292084.1 | ||
| NM_001305156.1 | 761 | Intron | NP_001292085.1 | ||
| NM_017917.3 | 761 | Intron | NP_060387.2 |