| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001104629.1 | 1025 | Missense Mutation | CCT,GCT | P260A | NP_001098099.1 |
| NM_018302.2 | 1025 | Missense Mutation | CCT,GCT | P260A | NP_060772.2 |
| XM_011513712.2 | 1025 | Missense Mutation | CCT,GCT | P260A | XP_011512014.1 |
| XM_011513713.2 | 1025 | Missense Mutation | CCT,GCT | P260A | XP_011512015.1 |
| XM_017008361.1 | 1025 | Missense Mutation | CCT,GCT | P260A | XP_016863850.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001085399.1 | 1025 | UTR 3 | NP_001078868.1 | ||
| NM_001085400.1 | 1025 | Intron | NP_001078869.1 | ||
| XM_017008590.1 | 1025 | Intron | XP_016864079.1 |