ENST00000539696.6:c.202G>T
|
ENSP00000439134.1:p.Glu68Ter
|
|
ENST00000546277.6:c.1045G>T
|
ENSP00000438153.2:p.Glu349Ter
|
|
ENST00000636529.2:n.684G>T
|
|
|
ENST00000697195.1:c.*809G>T
|
ENSP00000513181.1:n.*809G>T
|
|
ENST00000697196.1:c.*218G>T
|
ENSP00000513182.1:n.*218G>T
|
|
ENST00000697197.1:n.3074G>T
|
|
|
ENST00000697198.1:n.1429G>T
|
|
|
ENST00000228510.8:c.1045G>T
MANE Select
|
ENSP00000228510.3:p.Glu349Ter
|
|
ENST00000636529.1:c.670G>T
|
|
|
ENST00000636996.1:c.893G>T
|
|
|
ENST00000228510.7:c.1045G>T
|
ENSP00000228510.3:p.Glu349Ter
|
|
ENST00000392727.7:c.889G>T
|
ENSP00000376487.3:p.Glu297Ter
|
|
ENST00000447878.6:c.*492G>T
|
ENSP00000415555.2:n.*492G>T
|
|
ENST00000537237.5:c.*718G>T
|
ENSP00000445382.1:n.*718G>T
|
|
ENST00000539575.4:c.1045G>T
|
ENSP00000443551.2:p.Glu349Ter
|
|
ENST00000539696.5:c.202G>T
|
ENSP00000439134.1:p.Glu68Ter
|
|
ENST00000540353.1:n.3278G>T
|
|
|
ENST00000625889.2:c.889G>T
|
ENSP00000486846.1:p.Glu297Ter
|
|
ENST00000629016.2:c.*492G>T
|
ENSP00000486804.1:n.*492G>T
|
|
NM_000431.3:c.1045G>T
|
NP_000422.1:p.Glu349Ter
|
|
NM_001114185.2:c.1045G>T
|
NP_001107657.1:p.Glu349Ter
|
|
NM_001301182.1:c.889G>T
|
NP_001288111.1:p.Glu297Ter
|
|
XM_011538372.1:c.1045G>T
|
XP_011536674.1:p.Glu349Ter
|
|
XM_017019313.2:c.889G>T
|
XP_016874802.1:p.Glu297Ter
|
|
XM_017019314.1:c.1045G>T
|
XP_016874803.1:p.Glu349Ter
|
|
NM_000431.4:c.1045G>T
MANE Select
|
NP_000422.1:p.Glu349Ter
|
|
NM_001114185.3:c.1045G>T
|
NP_001107657.1:p.Glu349Ter
|
|
NM_001301182.2:c.889G>T
|
NP_001288111.1:p.Glu297Ter
|
|