ENST00000355520.6:c.239A>T
MANE Select
|
ENSP00000347710.5:p.Glu80Val
|
|
ENST00000679748.1:c.239A>T
|
ENSP00000505800.1:p.Glu80Val
|
|
ENST00000679822.1:c.239A>T
|
ENSP00000505810.1:p.Glu80Val
|
|
ENST00000679914.1:n.598A>T
|
|
|
ENST00000680417.1:n.60A>T
|
|
|
ENST00000680503.1:n.916A>T
|
|
|
ENST00000680612.1:c.239A>T
|
ENSP00000505365.1:p.Glu80Val
|
|
ENST00000681408.1:c.239A>T
|
ENSP00000506619.1:p.Glu80Val
|
|
ENST00000355520.5:c.239A>T
|
ENSP00000347710.5:p.Glu80Val
|
|
ENST00000486068.1:n.109A>T
|
|
|
NM_002547.2:c.239A>T
|
NP_002538.1:p.Glu80Val
|
|
XM_005262270.1:c.239A>T
|
XP_005262327.1:p.Glu80Val
|
|
XM_006724653.1:c.239A>T
|
XP_006724716.1:p.Glu80Val
|
|
XM_011530961.1:c.239A>T
|
XP_011529263.1:p.Glu80Val
|
|
XM_006724653.2:c.239A>T
|
XP_006724716.1:p.Glu80Val
|
|
XM_017029555.1:c.239A>T
|
XP_016885044.1:p.Glu80Val
|
|
NM_002547.3:c.239A>T
MANE Select
|
NP_002538.1:p.Glu80Val
|
|