ENST00000651066.1:c.*1086G>A
|
ENSP00000499143.1:n.*1086G>A
|
|
ENST00000651284.1:c.*573G>A
|
ENSP00000499064.1:n.*573G>A
|
|
ENST00000651899.1:c.*485G>A
|
ENSP00000498993.1:n.*485G>A
|
|
ENST00000652027.2:c.944G>A
MANE Select
|
ENSP00000499171.2:p.Cys315Tyr
|
|
ENST00000323833.12:c.1007G>A
|
ENSP00000313877.8:p.Cys336Tyr
|
|
ENST00000454289.7:c.944G>A
|
ENSP00000388330.2:p.Cys315Tyr
|
|
ENST00000540550.6:c.*352G>A
|
ENSP00000440987.1:n.*352G>A
|
|
ENST00000543727.5:c.571+3476G>A
|
ENSP00000439342.1:n.571+3476G>A
|
|
ENST00000548851.5:c.571+3476G>A
|
ENSP00000450041.1:n.571+3476G>A
|
|
ENST00000550559.5:c.571+3476G>A
|
ENSP00000448575.1:n.571+3476G>A
|
|
NM_001172695.1:c.*352G>A
|
NP_001166166.1:n.*352G>A
|
|
NM_001172696.1:c.1007G>A
|
NP_001166167.1:p.Cys336Tyr
|
|
NM_001172697.1:c.571+3476G>A
|
NP_001166168.1:n.571+3476G>A
|
|
NM_005726.5:c.944G>A
|
NP_005717.3:p.Cys315Tyr
|
|
NM_001172695.2:c.*352G>A
|
NP_001166166.1:n.*352G>A
|
|
NM_001172696.2:c.1007G>A
|
NP_001166167.1:p.Cys336Tyr
|
|
NM_005726.6:c.944G>A
MANE Select
|
NP_005717.3:p.Cys315Tyr
|
|
NM_001172697.2:c.571+3476G>A
|
NP_001166168.1:n.571+3476G>A
|
|