ENST00000409350.6:c.291A>T
|
ENSP00000386968.2:p.Glu97Asp
|
|
ENST00000439384.6:n.514A>T
|
|
|
ENST00000446446.6:c.252A>T
|
ENSP00000396867.2:p.Glu84Asp
|
|
ENST00000706158.1:c.*196A>T
|
ENSP00000516236.1:n.*196A>T
|
|
ENST00000706159.1:c.164A>T
|
ENSP00000516237.1:p.Lys55Ile
|
|
ENST00000706160.1:c.252A>T
|
ENSP00000516238.1:p.Glu84Asp
|
|
ENST00000706161.1:c.330A>T
|
ENSP00000516239.1:p.Glu110Asp
|
|
ENST00000706162.1:c.252A>T
|
ENSP00000516240.1:p.Glu84Asp
|
|
ENST00000706163.1:c.50-81831A>T
|
ENSP00000516241.1:n.50-81831A>T
|
|
ENST00000222792.11:c.252A>T
MANE Select
|
ENSP00000222792.7:p.Glu84Asp
|
|
ENST00000644824.1:c.477A>T
|
ENSP00000495614.1:p.Glu159Asp
|
|
ENST00000222792.10:c.252A>T
|
ENSP00000222792.6:p.Glu84Asp
|
|
ENST00000409350.5:c.291A>T
|
ENSP00000386968.1:p.Glu97Asp
|
|
ENST00000409922.5:n.463A>T
|
|
|
ENST00000409964.6:n.451A>T
|
|
|
ENST00000412536.5:n.272A>T
|
|
|
ENST00000435288.6:c.168+4746A>T
|
ENSP00000400282.3:n.168+4746A>T
|
|
ENST00000439384.5:c.477A>T
|
ENSP00000409843.1:p.Glu159Asp
|
|
ENST00000474070.5:c.352A>T
|
|
|
ENST00000478128.6:n.346A>T
|
|
|
ENST00000482820.6:n.461A>T
|
|
|
ENST00000491856.1:n.1801A>T
|
|
|
ENST00000495789.6:c.252A>T
|
ENSP00000438587.2:p.Glu84Asp
|
|
ENST00000539389.5:c.252A>T
|
ENSP00000440526.2:p.Glu84Asp
|
|
ENST00000539406.5:c.252A>T
|
ENSP00000444063.2:p.Glu84Asp
|
|
NM_001293069.1:c.477A>T
|
NP_001279998.1:p.Glu159Asp
|
|
NM_001293070.1:c.291A>T
|
NP_001279999.1:p.Glu97Asp
|
|
NM_001293071.1:c.147A>T
|
NP_001280000.1:p.Glu49Asp
|
|
NM_001293072.1:c.207A>T
|
NP_001280001.1:p.Glu69Asp
|
|
NM_004067.3:c.252A>T
|
NP_004058.1:p.Glu84Asp
|
|
XM_011515105.1:c.555A>T
|
XP_011513407.1:p.Glu185Asp
|
|
XM_011515106.1:c.516A>T
|
XP_011513408.1:p.Glu172Asp
|
|
XM_011515107.1:c.330A>T
|
XP_011513409.1:p.Glu110Asp
|
|
XM_011515108.1:c.252A>T
|
XP_011513410.1:p.Glu84Asp
|
|
XM_011515109.1:c.213A>T
|
XP_011513411.1:p.Glu71Asp
|
|
XM_011515110.1:c.174A>T
|
XP_011513412.1:p.Glu58Asp
|
|
XM_011515111.1:c.147A>T
|
XP_011513413.1:p.Glu49Asp
|
|
XM_011515112.1:c.555A>T
|
XP_011513414.1:p.Glu185Asp
|
|
XM_011515105.2:c.555A>T
|
XP_011513407.1:p.Glu185Asp
|
|
XM_011515106.2:c.516A>T
|
XP_011513408.1:p.Glu172Asp
|
|
XM_011515107.2:c.330A>T
|
XP_011513409.1:p.Glu110Asp
|
|
XM_017011721.1:c.573A>T
|
XP_016867210.1:p.Glu191Asp
|
|
XM_017011722.1:c.348A>T
|
XP_016867211.1:p.Glu116Asp
|
|
NM_004067.4:c.252A>T
MANE Select
|
NP_004058.1:p.Glu84Asp
|
|
NM_001293070.2:c.291A>T
|
NP_001279999.1:p.Glu97Asp
|
|
NM_001293071.2:c.147A>T
|
NP_001280000.1:p.Glu49Asp
|
|
NM_001293072.2:c.207A>T
|
NP_001280001.1:p.Glu69Asp
|
|
NM_001398427.1:c.-187A>T
|
NP_001385356.1:n.-187A>T
|
|