ENST00000682424.1:c.640G>T
|
ENSP00000507321.1:p.Ala214Ser
|
|
ENST00000299427.12:c.754G>T
MANE Select
|
ENSP00000299427.6:p.Ala252Ser
|
|
ENST00000436873.7:c.312+508G>T
|
|
|
ENST00000524788.2:n.1913G>T
|
|
|
ENST00000524903.2:n.2029G>T
|
|
|
ENST00000528807.2:n.410G>T
|
|
|
ENST00000530040.2:n.480-290G>T
|
|
|
ENST00000533371.6:c.25G>T
|
ENSP00000437066.1:p.Ala9Ser
|
|
ENST00000642892.1:c.25G>T
|
ENSP00000494165.1:p.Ala9Ser
|
|
ENST00000643439.1:c.*494G>T
|
ENSP00000495849.1:n.*494G>T
|
|
ENST00000643479.1:n.783G>T
|
|
|
ENST00000643516.1:c.396-290G>T
|
|
|
ENST00000644151.1:n.2193G>T
|
|
|
ENST00000644218.1:c.754G>T
|
ENSP00000493574.1:p.Ala252Ser
|
|
ENST00000644683.1:c.*207G>T
|
ENSP00000494085.1:n.*207G>T
|
|
ENST00000644810.1:c.475G>T
|
ENSP00000495895.1:p.Ala159Ser
|
|
ENST00000644831.1:n.930G>T
|
|
|
ENST00000644933.1:c.25G>T
|
ENSP00000496133.1:p.Ala9Ser
|
|
ENST00000645020.1:n.2044G>T
|
|
|
ENST00000645285.1:c.25G>T
|
ENSP00000495058.1:p.Ala9Ser
|
|
ENST00000645331.1:n.1120G>T
|
|
|
ENST00000645620.1:c.25G>T
|
ENSP00000493657.1:p.Ala9Ser
|
|
ENST00000646777.1:n.930G>T
|
|
|
ENST00000647016.1:n.1234G>T
|
|
|
ENST00000647152.1:c.25G>T
|
ENSP00000495893.1:p.Ala9Ser
|
|
ENST00000647209.1:c.*623G>T
|
ENSP00000495558.1:n.*623G>T
|
|
ENST00000647346.1:n.1774G>T
|
|
|
ENST00000299427.10:c.754G>T
|
ENSP00000299427.6:p.Ala252Ser
|
|
ENST00000436873.6:c.451-290G>T
|
ENSP00000398136.2:n.451-290G>T
|
|
ENST00000524788.1:n.454G>T
|
|
|
ENST00000528807.1:n.304G>T
|
|
|
ENST00000533371.5:c.25G>T
|
ENSP00000437066.1:p.Ala9Ser
|
|
ENST00000611494.4:c.754G>T
|
ENSP00000484546.1:p.Ala252Ser
|
|
NM_000391.3:c.754G>T
|
NP_000382.3:p.Ala252Ser
|
|
NM_000391.4:c.754G>T
MANE Select
|
NP_000382.3:p.Ala252Ser
|
|