|
NM_001754.5:c.849G>T
MANE Select
|
NP_001745.2:p.Gln283His
|
|
ENST00000675419.1:c.849G>T
MANE Select
|
ENSP00000501943.1:p.Gln283His
|
|
NM_001001890.2:c.768G>T
|
NP_001001890.1:p.Gln256His
|
|
NM_001001890.3:c.768G>T
|
NP_001001890.1:p.Gln256His
|
|
NM_001754.4:c.849G>T , LRG_482t1:c.849G>T
|
NP_001745.2:p.Gln283His
|
|
ENST00000300305.7:c.849G>T
|
ENSP00000300305.3:p.Gln283His
|
|
ENST00000344691.8:c.768G>T
|
ENSP00000340690.4:p.Gln256His
|
|
ENST00000399240.5:c.576G>T
|
ENSP00000382184.1:p.Gln192His
|
|
ENST00000437180.5:c.849G>T
|
ENSP00000409227.1:p.Gln283His
|
|
ENST00000482318.5:c.*439G>T
|
ENSP00000477067.1:n.*439G>T
|
|
XM_005261068.3:c.813G>T
|
XP_005261125.1:p.Gln271His
|
|
XM_005261069.3:c.657G>T
|
XP_005261126.1:p.Gln219His
|
|
XM_005261069.4:c.657G>T
|
XP_005261126.1:p.Gln219His
|
|
XM_011529766.1:c.849G>T
|
XP_011528068.1:p.Gln283His
|
|
XM_011529766.2:c.849G>T
|
XP_011528068.1:p.Gln283His
|
|
XM_011529767.1:c.810G>T
|
XP_011528069.1:p.Gln270His
|
|
XM_011529767.2:c.810G>T
|
XP_011528069.1:p.Gln270His
|
|
XM_011529768.1:c.618G>T
|
XP_011528070.1:p.Gln206His
|
|
XM_011529768.2:c.618G>T
|
XP_011528070.1:p.Gln206His
|
|
XM_017028487.1:c.696G>T
|
XP_016883976.1:p.Gln232His
|
|
XR_937576.1:n.1028G>T
|
|
|
XR_937576.2:n.1075G>T
|
|
