Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001303472.1 | 448 | UTR 5 | NP_001290401.1 | ||
NM_022096.5 | 448 | Missense Mutation | GCT,GTT | A2V | NP_071379.3 |
NM_198798.2 | 448 | Missense Mutation | GCT,GTT | A2V | NP_942093.1 |
XM_005260792.2 | 448 | Intron | XP_005260849.1 |