| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004857.3 | 1042 | Missense Mutation | CCT,GCT | P222A | NP_004848.3 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304507.1 | 1042 | Intron | NP_001291436.1 | ||
| NM_001304508.1 | 1042 | Intron | NP_001291437.1 | ||
| NM_006977.3 | 1042 | Intron | NP_008908.2 | ||
| XM_005268051.3 | 1042 | Intron | XP_005268108.1 | ||
| XM_006720250.3 | 1042 | Intron | XP_006720313.1 | ||
| XM_006720251.3 | 1042 | Intron | XP_006720314.1 | ||
| XM_006720252.3 | 1042 | Intron | XP_006720315.1 | ||
| XM_011537139.1 | 1042 | Intron | XP_011535441.1 | ||
| XM_011537141.2 | 1042 | Intron | XP_011535443.1 | ||
| XM_011537143.2 | 1042 | Intron | XP_011535445.1 | ||
| XM_011537146.2 | 1042 | Intron | XP_011535448.1 | ||
| XM_017021630.1 | 1042 | Intron | XP_016877119.1 | ||
| XM_017021631.1 | 1042 | Intron | XP_016877120.1 | ||
| XM_017021632.1 | 1042 | Intron | XP_016877121.1 | ||
| XM_017021633.1 | 1042 | Intron | XP_016877122.1 | ||
| XM_017021634.1 | 1042 | Intron | XP_016877123.1 | ||
| XM_017021635.1 | 1042 | Intron | XP_016877124.1 | ||
| XM_017021636.1 | 1042 | Intron | XP_016877125.1 | ||
| XM_017021637.1 | 1042 | Intron | XP_016877126.1 | ||
| XM_017021638.1 | 1042 | Intron | XP_016877127.1 |