|
ENST00000476680.2:c.318-4140A=
|
|
|
|
ENST00000537320.6:c.3215-4140A=
|
ENSP00000443478.1:n.3215-4140A=
|
|
|
ENST00000542877.6:c.3965A=
|
ENSP00000442242.1:p.Glu1322=
|
|
|
ENST00000705190.1:c.1997A=
|
ENSP00000516083.1:p.Glu666=
|
|
|
ENST00000705191.1:c.653A=
|
ENSP00000516084.1:p.Glu218=
|
|
|
ENST00000705192.1:c.4012A=
|
|
|
|
ENST00000350763.9:c.5054A=
MANE Select
|
ENSP00000265131.4:p.Glu1685=
|
|
|
ENST00000341037.8:c.4508A=
|
ENSP00000339553.4:p.Glu1503=
|
|
|
ENST00000350763.8:c.5054A=
|
ENSP00000265131.4:p.Glu1685=
|
|
|
ENST00000423613.6:c.4307-4140A=
|
ENSP00000411406.2:n.4307-4140A=
|
|
|
ENST00000473855.1:n.372A=
|
|
|
|
ENST00000476680.1:n.253-4140A=
|
|
|
|
ENST00000498724.5:n.40-4140A=
|
|
|
|
ENST00000535648.5:c.3965A=
|
ENSP00000438152.2:p.Glu1322=
|
|
|
ENST00000537320.5:c.3215-4140A=
|
ENSP00000443478.1:n.3215-4140A=
|
|
|
ENST00000542877.5:c.3965A=
|
ENSP00000442242.1:p.Glu1322=
|
|
|
ENST00000544972.1:c.741A=
|
|
|
|
NM_002160.3:c.5054A=
|
NP_002151.2:p.Glu1685=
|
|
|
XM_005251972.2:c.4781A=
|
XP_005252029.1:p.Glu1594=
|
|
|
XM_005251973.2:c.4034-4140A=
|
XP_005252030.1:n.4034-4140A=
|
|
|
XM_005251974.2:c.3416A=
|
XP_005252031.1:p.Glu1139=
|
|
|
XM_005251975.2:c.3215-4140A=
|
XP_005252032.1:n.3215-4140A=
|
|
|
XM_006717096.2:c.5330A=
|
XP_006717159.1:p.Glu1777=
|
|
|
XM_006717097.2:c.4781A=
|
XP_006717160.1:p.Glu1594=
|
|
|
XM_006717098.2:c.4508A=
|
XP_006717161.1:p.Glu1503=
|
|
|
XM_006717100.2:c.4307-4140A=
|
XP_006717163.1:n.4307-4140A=
|
|
|
XM_006717101.2:c.3488-4140A=
|
XP_006717164.1:n.3488-4140A=
|
|
|
XM_011518622.1:c.5057A=
|
XP_011516924.1:p.Glu1686=
|
|
|
XM_011518623.1:c.5057A=
|
XP_011516925.1:p.Glu1686=
|
|
|
XM_011518624.1:c.4511A=
|
XP_011516926.1:p.Glu1504=
|
|
|
XM_011518625.1:c.4580-4140A=
|
XP_011516927.1:n.4580-4140A=
|
|
|
XM_011518626.1:c.4238A=
|
XP_011516928.1:p.Glu1413=
|
|
|
XM_011518627.1:c.3965A=
|
XP_011516929.1:p.Glu1322=
|
|
|
XM_011518628.1:c.3761-4140A=
|
XP_011516930.1:n.3761-4140A=
|
|
|
XM_011518629.1:c.3689A=
|
XP_011516931.1:p.Glu1230=
|
|
|
XM_005251972.4:c.4781A=
|
XP_005252029.1:p.Glu1594=
|
|
|
XM_005251973.4:c.4034-4140A=
|
XP_005252030.1:n.4034-4140A=
|
|
|
XM_005251974.4:c.3416A=
|
XP_005252031.1:p.Glu1139=
|
|
|
XM_005251975.4:c.3215-4140A=
|
XP_005252032.1:n.3215-4140A=
|
|
|
XM_006717096.4:c.5330A=
|
XP_006717159.1:p.Glu1777=
|
|
|
XM_006717097.4:c.4781A=
|
XP_006717160.1:p.Glu1594=
|
|
|
XM_006717098.4:c.4508A=
|
XP_006717161.1:p.Glu1503=
|
|
|
XM_006717101.4:c.3488-4140A=
|
XP_006717164.1:n.3488-4140A=
|
|
|
XM_011518625.3:c.4580-4140A=
|
XP_011516927.1:n.4580-4140A=
|
|
|
XM_011518626.3:c.4238A=
|
XP_011516928.1:p.Glu1413=
|
|
|
XM_011518628.3:c.3761-4140A=
|
XP_011516930.1:n.3761-4140A=
|
|
|
XM_011518629.3:c.3689A=
|
XP_011516931.1:p.Glu1230=
|
|
|
XM_017014678.2:c.5603A=
|
XP_016870167.1:p.Glu1868=
|
|
|
XM_017014679.2:c.5330A=
|
XP_016870168.1:p.Glu1777=
|
|
|
XM_017014680.2:c.5327A=
|
XP_016870169.1:p.Glu1776=
|
|
|
XM_017014681.2:c.4511A=
|
XP_016870170.1:p.Glu1504=
|
|
|
XM_024447530.1:c.5603A=
|
XP_024303298.1:p.Glu1868=
|
|
|
NM_002160.4:c.5054A=
MANE Select
|
NP_002151.2:p.Glu1685=
|
|
