ENST00000526209.2:c.288G>T
|
|
|
ENST00000681974.1:n.990G>T
|
|
|
ENST00000682693.1:n.1952G>T
|
|
|
ENST00000682886.1:n.488G>T
|
|
|
ENST00000683543.2:c.16366G>T
|
ENSP00000506726.1:p.Glu5456Ter
|
|
ENST00000683988.1:c.289G>T
|
ENSP00000506939.1:p.Glu97Ter
|
|
ENST00000684428.1:c.853G>T
|
ENSP00000507433.1:p.Glu285Ter
|
|
ENST00000684755.1:n.901G>T
|
|
|
ENST00000685024.1:c.1472G>T
|
|
|
ENST00000685166.1:c.16327G>T
|
ENSP00000509386.1:p.Glu5443Ter
|
|
ENST00000688411.1:c.795G>T
|
ENSP00000510146.1:n.795G>T
|
|
ENST00000691932.1:c.319G>T
|
ENSP00000509037.1:p.Glu107Ter
|
|
ENST00000692637.1:c.16315G>T
|
ENSP00000509666.1:p.Glu5439Ter
|
|
ENST00000301067.12:c.16318G>T
MANE Select
|
ENSP00000301067.7:p.Glu5440Ter
|
|
ENST00000301067.11:c.16318G>T
|
ENSP00000301067.7:p.Glu5440Ter
|
|
ENST00000526209.1:c.361G>T
|
ENSP00000435714.1:p.Glu121Ter
|
|
NM_003482.3:c.16318G>T
|
NP_003473.3:p.Glu5440Ter
|
|
XM_005269162.3:c.16318G>T
|
XP_005269219.1:p.Glu5440Ter
|
|
XM_006719614.2:c.16327G>T
|
XP_006719677.1:p.Glu5443Ter
|
|
XM_006719616.2:c.16315G>T
|
XP_006719679.1:p.Glu5439Ter
|
|
XM_011538770.1:c.16375G>T
|
XP_011537072.1:p.Glu5459Ter
|
|
XM_011538771.1:c.16372G>T
|
XP_011537073.1:p.Glu5458Ter
|
|
XM_011538772.1:c.16366G>T
|
XP_011537074.1:p.Glu5456Ter
|
|
XM_011538773.1:c.16363G>T
|
XP_011537075.1:p.Glu5455Ter
|
|
XM_011538774.1:c.16354G>T
|
XP_011537076.1:p.Glu5452Ter
|
|
XM_011538775.1:c.16309G>T
|
XP_011537077.1:p.Glu5437Ter
|
|
XM_011538776.1:c.16282G>T
|
XP_011537078.1:p.Glu5428Ter
|
|
XM_005269162.4:c.16318G>T
|
XP_005269219.1:p.Glu5440Ter
|
|
XM_006719614.4:c.16327G>T
|
XP_006719677.1:p.Glu5443Ter
|
|
XM_006719616.3:c.16315G>T
|
XP_006719679.1:p.Glu5439Ter
|
|
XM_011538770.2:c.16375G>T
|
XP_011537072.1:p.Glu5459Ter
|
|
XM_011538771.2:c.16372G>T
|
XP_011537073.1:p.Glu5458Ter
|
|
XM_011538772.2:c.16366G>T
|
XP_011537074.1:p.Glu5456Ter
|
|
XM_011538773.2:c.16363G>T
|
XP_011537075.1:p.Glu5455Ter
|
|
XM_011538774.2:c.16354G>T
|
XP_011537076.1:p.Glu5452Ter
|
|
XM_011538776.2:c.16282G>T
|
XP_011537078.1:p.Glu5428Ter
|
|
XR_001748874.1:n.16495G>T
|
|
|
NM_003482.4:c.16318G>T
MANE Select
|
NP_003473.3:p.Glu5440Ter
|
|