Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003190.4 | 1807 | Intron | NP_003181.3 | ||
NM_172208.2 | 1807 | Missense Mutation | TGC,TGG | C487W | NP_757345.2 |
NM_172209.2 | 1807 | Intron | NP_757346.2 | ||
XM_011514828.2 | 1807 | Intron | XP_011513130.1 | ||
XM_017011227.1 | 1807 | Intron | XP_016866716.1 |