ENST00000526209.2:c.290G>T
|
|
|
ENST00000681974.1:n.992G>T
|
|
|
ENST00000682693.1:n.1954G>T
|
|
|
ENST00000682886.1:n.490G>T
|
|
|
ENST00000683543.2:c.16368G>T
|
ENSP00000506726.1:p.Glu5456Asp
|
|
ENST00000683988.1:c.291G>T
|
ENSP00000506939.1:p.Glu97Asp
|
|
ENST00000684428.1:c.855G>T
|
ENSP00000507433.1:p.Glu285Asp
|
|
ENST00000684755.1:n.903G>T
|
|
|
ENST00000685024.1:c.1474G>T
|
|
|
ENST00000685166.1:c.16329G>T
|
ENSP00000509386.1:p.Glu5443Asp
|
|
ENST00000688411.1:c.797G>T
|
ENSP00000510146.1:n.797G>T
|
|
ENST00000691932.1:c.321G>T
|
ENSP00000509037.1:p.Glu107Asp
|
|
ENST00000692637.1:c.16317G>T
|
ENSP00000509666.1:p.Glu5439Asp
|
|
ENST00000301067.12:c.16320G>T
MANE Select
|
ENSP00000301067.7:p.Glu5440Asp
|
|
ENST00000301067.11:c.16320G>T
|
ENSP00000301067.7:p.Glu5440Asp
|
|
ENST00000526209.1:c.363G>T
|
ENSP00000435714.1:p.Glu121Asp
|
|
NM_003482.3:c.16320G>T
|
NP_003473.3:p.Glu5440Asp
|
|
XM_005269162.3:c.16320G>T
|
XP_005269219.1:p.Glu5440Asp
|
|
XM_006719614.2:c.16329G>T
|
XP_006719677.1:p.Glu5443Asp
|
|
XM_006719616.2:c.16317G>T
|
XP_006719679.1:p.Glu5439Asp
|
|
XM_011538770.1:c.16377G>T
|
XP_011537072.1:p.Glu5459Asp
|
|
XM_011538771.1:c.16374G>T
|
XP_011537073.1:p.Glu5458Asp
|
|
XM_011538772.1:c.16368G>T
|
XP_011537074.1:p.Glu5456Asp
|
|
XM_011538773.1:c.16365G>T
|
XP_011537075.1:p.Glu5455Asp
|
|
XM_011538774.1:c.16356G>T
|
XP_011537076.1:p.Glu5452Asp
|
|
XM_011538775.1:c.16311G>T
|
XP_011537077.1:p.Glu5437Asp
|
|
XM_011538776.1:c.16284G>T
|
XP_011537078.1:p.Glu5428Asp
|
|
XM_005269162.4:c.16320G>T
|
XP_005269219.1:p.Glu5440Asp
|
|
XM_006719614.4:c.16329G>T
|
XP_006719677.1:p.Glu5443Asp
|
|
XM_006719616.3:c.16317G>T
|
XP_006719679.1:p.Glu5439Asp
|
|
XM_011538770.2:c.16377G>T
|
XP_011537072.1:p.Glu5459Asp
|
|
XM_011538771.2:c.16374G>T
|
XP_011537073.1:p.Glu5458Asp
|
|
XM_011538772.2:c.16368G>T
|
XP_011537074.1:p.Glu5456Asp
|
|
XM_011538773.2:c.16365G>T
|
XP_011537075.1:p.Glu5455Asp
|
|
XM_011538774.2:c.16356G>T
|
XP_011537076.1:p.Glu5452Asp
|
|
XM_011538776.2:c.16284G>T
|
XP_011537078.1:p.Glu5428Asp
|
|
XR_001748874.1:n.16497G>T
|
|
|
NM_003482.4:c.16320G>T
MANE Select
|
NP_003473.3:p.Glu5440Asp
|
|