| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271022.1 | 1041 | Intron | NP_001257951.1 | ||
| NM_001271023.1 | 1041 | Intron | NP_001257952.1 | ||
| NM_032166.3 | 1041 | Intron | NP_115542.2 | ||
| NM_130384.2 | 1041 | Intron | NP_569055.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_007248.3 | 1041 | Intron | NP_009179.2 | ||
| NM_016381.5 | 1041 | Missense Mutation | CCT,GCT | P24A | NP_057465.1 |
| NM_033629.4 | 1041 | Intron | NP_338599.1 |