| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004125.3 | 471 | Missense Mutation | CCT,GCT | P139A | NP_004116.2 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001017998.3 | 471 | Intron | NP_001017998.1 | ||
| NM_001198664.1 | 471 | Intron | NP_001185593.1 |