ENST00000526209.2:c.288G>A
|
|
|
ENST00000681974.1:n.990G>A
|
|
|
ENST00000682693.1:n.1952G>A
|
|
|
ENST00000682886.1:n.488G>A
|
|
|
ENST00000683543.2:c.16366G>A
|
ENSP00000506726.1:p.Glu5456Lys
|
|
ENST00000683988.1:c.289G>A
|
ENSP00000506939.1:p.Glu97Lys
|
|
ENST00000684428.1:c.853G>A
|
ENSP00000507433.1:p.Glu285Lys
|
|
ENST00000684755.1:n.901G>A
|
|
|
ENST00000685024.1:c.1472G>A
|
|
|
ENST00000685166.1:c.16327G>A
|
ENSP00000509386.1:p.Glu5443Lys
|
|
ENST00000688411.1:c.795G>A
|
ENSP00000510146.1:n.795G>A
|
|
ENST00000691932.1:c.319G>A
|
ENSP00000509037.1:p.Glu107Lys
|
|
ENST00000692637.1:c.16315G>A
|
ENSP00000509666.1:p.Glu5439Lys
|
|
ENST00000301067.12:c.16318G>A
MANE Select
|
ENSP00000301067.7:p.Glu5440Lys
|
|
ENST00000301067.11:c.16318G>A
|
ENSP00000301067.7:p.Glu5440Lys
|
|
ENST00000526209.1:c.361G>A
|
ENSP00000435714.1:p.Glu121Lys
|
|
NM_003482.3:c.16318G>A
|
NP_003473.3:p.Glu5440Lys
|
|
XM_005269162.3:c.16318G>A
|
XP_005269219.1:p.Glu5440Lys
|
|
XM_006719614.2:c.16327G>A
|
XP_006719677.1:p.Glu5443Lys
|
|
XM_006719616.2:c.16315G>A
|
XP_006719679.1:p.Glu5439Lys
|
|
XM_011538770.1:c.16375G>A
|
XP_011537072.1:p.Glu5459Lys
|
|
XM_011538771.1:c.16372G>A
|
XP_011537073.1:p.Glu5458Lys
|
|
XM_011538772.1:c.16366G>A
|
XP_011537074.1:p.Glu5456Lys
|
|
XM_011538773.1:c.16363G>A
|
XP_011537075.1:p.Glu5455Lys
|
|
XM_011538774.1:c.16354G>A
|
XP_011537076.1:p.Glu5452Lys
|
|
XM_011538775.1:c.16309G>A
|
XP_011537077.1:p.Glu5437Lys
|
|
XM_011538776.1:c.16282G>A
|
XP_011537078.1:p.Glu5428Lys
|
|
XM_005269162.4:c.16318G>A
|
XP_005269219.1:p.Glu5440Lys
|
|
XM_006719614.4:c.16327G>A
|
XP_006719677.1:p.Glu5443Lys
|
|
XM_006719616.3:c.16315G>A
|
XP_006719679.1:p.Glu5439Lys
|
|
XM_011538770.2:c.16375G>A
|
XP_011537072.1:p.Glu5459Lys
|
|
XM_011538771.2:c.16372G>A
|
XP_011537073.1:p.Glu5458Lys
|
|
XM_011538772.2:c.16366G>A
|
XP_011537074.1:p.Glu5456Lys
|
|
XM_011538773.2:c.16363G>A
|
XP_011537075.1:p.Glu5455Lys
|
|
XM_011538774.2:c.16354G>A
|
XP_011537076.1:p.Glu5452Lys
|
|
XM_011538776.2:c.16282G>A
|
XP_011537078.1:p.Glu5428Lys
|
|
XR_001748874.1:n.16495G>A
|
|
|
NM_003482.4:c.16318G>A
MANE Select
|
NP_003473.3:p.Glu5440Lys
|
|