ENST00000706952.1:c.1016C>A
|
ENSP00000516672.1:p.Ala339Asp
|
|
ENST00000638630.1:c.146C>A
|
ENSP00000492390.1:p.Ala49Asp
|
|
ENST00000640694.1:c.857C>A
|
ENSP00000492403.1:p.Ala286Asp
|
|
ENST00000642864.1:c.857C>A
MANE Select
|
ENSP00000495726.1:p.Ala286Asp
|
|
ENST00000674510.1:c.857C>A
|
ENSP00000502054.1:p.Ala286Asp
|
|
ENST00000675719.1:c.827C>A
|
ENSP00000501927.1:p.Ala276Asp
|
|
ENST00000375365.2:c.242C>A
|
ENSP00000364514.2:p.Ala81Asp
|
|
ENST00000396435.7:c.857C>A
|
ENSP00000379712.3:p.Ala286Asp
|
|
NM_001111125.2:c.857C>A
|
NP_001104595.1:p.Ala286Asp
|
|
NM_015075.1:c.242C>A
|
NP_055890.1:p.Ala81Asp
|
|
XM_006724579.2:c.953C>A
|
XP_006724642.1:p.Ala318Asp
|
|
XM_006724580.2:c.242C>A
|
XP_006724643.1:p.Ala81Asp
|
|
XM_006724581.2:c.953C>A
|
XP_006724644.1:p.Ala318Asp
|
|
XM_006724582.2:c.953C>A
|
XP_006724645.1:p.Ala318Asp
|
|
XM_006724583.2:c.953C>A
|
XP_006724646.1:p.Ala318Asp
|
|
XM_006724584.2:c.953C>A
|
XP_006724647.1:p.Ala318Asp
|
|
XM_011530772.1:c.179C>A
|
XP_011529074.1:p.Ala60Asp
|
|
XM_011530773.1:c.146C>A
|
XP_011529075.1:p.Ala49Asp
|
|
XM_011530774.1:c.953C>A
|
XP_011529076.1:p.Ala318Asp
|
|
XM_011530775.1:c.953C>A
|
XP_011529077.1:p.Ala318Asp
|
|
XM_011530776.1:c.953C>A
|
XP_011529078.1:p.Ala318Asp
|
|
XM_011530777.1:c.953C>A
|
XP_011529079.1:p.Ala318Asp
|
|
XR_938365.1:n.1180C>A
|
|
|
XM_006724579.3:c.953C>A
|
XP_006724642.1:p.Ala318Asp
|
|
XM_006724580.3:c.242C>A
|
XP_006724643.1:p.Ala81Asp
|
|
XM_006724581.4:c.953C>A
|
XP_006724644.1:p.Ala318Asp
|
|
XM_006724582.4:c.953C>A
|
XP_006724645.1:p.Ala318Asp
|
|
XM_006724583.4:c.953C>A
|
XP_006724646.1:p.Ala318Asp
|
|
XM_006724584.3:c.953C>A
|
XP_006724647.1:p.Ala318Asp
|
|
XM_011530773.2:c.146C>A
|
XP_011529075.1:p.Ala49Asp
|
|
XM_011530774.3:c.953C>A
|
XP_011529076.1:p.Ala318Asp
|
|
XM_011530776.2:c.953C>A
|
XP_011529078.1:p.Ala318Asp
|
|
XM_011530777.2:c.953C>A
|
XP_011529079.1:p.Ala318Asp
|
|
XM_017029359.2:c.827C>A
|
XP_016884848.1:p.Ala276Asp
|
|
XM_017029360.1:c.359C>A
|
XP_016884849.1:p.Ala120Asp
|
|
XR_938365.2:n.1174C>A
|
|
|
NM_001111125.3:c.857C>A
MANE Select
|
NP_001104595.1:p.Ala286Asp
|
|
NM_015075.2:c.242C>A
|
NP_055890.1:p.Ala81Asp
|
|