ENST00000685781.1:c.237+373G>A
MANE Select
|
ENSP00000509445.1:n.237+373G>A
|
|
ENST00000375331.7:c.237+373G>A
|
ENSP00000364480.3:n.237+373G>A
|
|
ENST00000375333.3:c.237+373G>A
|
ENSP00000364482.3:n.237+373G>A
|
|
ENST00000483801.6:c.100+619G>A
|
ENSP00000418866.2:n.100+619G>A
|
|
ENST00000519179.6:c.100+619G>A
|
ENSP00000454870.2:n.100+619G>A
|
|
ENST00000375331.6:c.567+373G>A
|
ENSP00000364480.2:n.567+373G>A
|
|
ENST00000375333.2:c.567+373G>A
|
ENSP00000364482.2:n.567+373G>A
|
|
ENST00000463823.5:n.138+619G>A
|
|
|
ENST00000466132.5:n.964+373G>A
|
|
|
ENST00000466336.5:n.252+373G>A
|
|
|
ENST00000469907.1:n.338+211G>A
|
|
|
ENST00000471028.1:n.223+373G>A
|
|
|
ENST00000473983.5:n.309+373G>A
|
|
|
ENST00000478486.5:n.459+211G>A
|
|
|
ENST00000479644.1:n.1106G>A
|
|
|
ENST00000483801.5:c.131+619G>A
|
|
|
ENST00000484540.5:n.180+373G>A
|
|
|
ENST00000491861.5:n.203+373G>A
|
|
|
ENST00000492583.5:n.750+373G>A
|
|
|
ENST00000519179.5:c.131+619G>A
|
|
|
NM_004197.1:c.567+373G>A
|
NP_004188.1:n.567+373G>A
|
|
NM_032454.1:c.567+373G>A
|
NP_115830.1:n.567+373G>A
|
|
NR_026717.1:n.880+373G>A
|
|
|
NM_004197.2:c.237+373G>A
MANE Select
|
NP_004188.2:n.237+373G>A
|
|