| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001172128.1 | 1182 | Intron | NP_001165599.1 | ||
| NM_004513.5 | 1182 | Intron | NP_004504.3 | ||
| NM_172217.3 | 1182 | Intron | NP_757366.2 | ||
| XM_005254342.3 | 1182 | Intron | XP_005254399.1 | ||
| XM_005254346.4 | 1182 | Intron | XP_005254403.1 | ||
| XM_011521519.2 | 1182 | Intron | XP_011519821.1 | ||
| XM_011521520.2 | 1182 | Intron | XP_011519822.1 | ||
| XM_017022140.1 | 1182 | Intron | XP_016877629.1 | ||
| XM_017022141.1 | 1182 | Intron | XP_016877630.1 | ||
| XM_017022142.1 | 1182 | Intron | XP_016877631.1 | ||
| XM_017022143.1 | 1182 | Intron | XP_016877632.1 | ||
| XM_017022144.1 | 1182 | Intron | XP_016877633.1 | ||
| XM_017022145.1 | 1182 | Intron | XP_016877634.1 | ||
| XM_017022146.1 | 1182 | Intron | XP_016877635.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_181900.2 | 1182 | Missense Mutation | CGC,TGC | R195C | NP_871629.1 |
| XM_006720703.1 | 1182 | Intron | XP_006720766.1 | ||
| XM_017022639.1 | 1182 | Missense Mutation | CGC,TGC | R174C | XP_016878128.1 |