ENST00000380743.9:c.842G>T
MANE Select
|
ENSP00000370119.4:p.Arg281Ile
|
|
ENST00000380741.8:c.842G>T
|
ENSP00000370117.5:p.Arg281Ile
|
|
ENST00000380742.8:c.746G>T
|
ENSP00000370118.4:p.Arg249Ile
|
|
ENST00000380743.8:c.842G>T
|
ENSP00000370119.4:p.Arg281Ile
|
|
ENST00000505346.5:n.308G>T
|
|
|
ENST00000506734.5:c.*59-491G>T
|
ENSP00000424799.1:n.*59-491G>T
|
|
ENST00000507458.2:c.96G>T
|
|
|
ENST00000511812.5:c.641G>T
|
ENSP00000424282.1:p.Arg214Ile
|
|
ENST00000514914.1:n.383G>T
|
|
|
ENST00000614240.4:c.746G>T
|
ENSP00000479279.1:p.Arg249Ile
|
|
ENST00000626847.2:c.835-491G>T
|
ENSP00000486152.1:n.835-491G>T
|
|
NM_017411.3:c.842G>T
|
NP_059107.1:p.Arg281Ile
|
|
NM_022875.2:c.835-491G>T
|
NP_075013.1:n.835-491G>T
|
|
NM_022876.2:c.746G>T
|
NP_075014.1:p.Arg249Ile
|
|
NM_022877.2:c.739-491G>T
|
NP_075015.1:n.739-491G>T
|
|
XM_011543600.1:c.641G>T
|
XP_011541902.1:p.Arg214Ile
|
|
XM_011543601.1:c.634-491G>T
|
XP_011541903.1:n.634-491G>T
|
|
XM_011543602.1:c.545G>T
|
XP_011541904.1:p.Arg182Ile
|
|
XM_011543603.1:c.538-491G>T
|
XP_011541905.1:n.538-491G>T
|
|
XR_948432.1:n.1054+88524G>T
|
|
|
XM_011543600.2:c.641G>T
|
XP_011541902.1:p.Arg214Ile
|
|
XM_011543602.3:c.545G>T
|
XP_011541904.1:p.Arg182Ile
|
|
XM_011543603.3:c.538-491G>T
|
XP_011541905.1:n.538-491G>T
|
|
NM_017411.4:c.842G>T
MANE Select
|
NP_059107.1:p.Arg281Ile
|
|
NM_022875.3:c.835-491G>T
|
NP_075013.1:n.835-491G>T
|
|