| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001297436.1 | 1279 | Missense Mutation | CGC,TGC | R456C | NP_001284365.1 |
| NM_001523.3 | 1279 | Missense Mutation | CGC,TGC | R457C | NP_001514.2 |
| XM_011526884.2 | 1279 | UTR 3 | XP_011525186.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001316972.1 | 1279 | Intron | NP_001303901.1 | ||
| NM_001316994.1 | 1279 | Intron | NP_001303923.1 |