ENST00000526209.2:c.301A>T
|
|
|
ENST00000681974.1:n.1003A>T
|
|
|
ENST00000682693.1:n.1965A>T
|
|
|
ENST00000682886.1:n.501A>T
|
|
|
ENST00000683543.2:c.16379A>T
|
ENSP00000506726.1:p.Glu5460Val
|
|
ENST00000683988.1:c.302A>T
|
ENSP00000506939.1:p.Glu101Val
|
|
ENST00000684428.1:c.866A>T
|
ENSP00000507433.1:p.Glu289Val
|
|
ENST00000684755.1:n.914A>T
|
|
|
ENST00000685024.1:c.1485A>T
|
|
|
ENST00000685166.1:c.16340A>T
|
ENSP00000509386.1:p.Glu5447Val
|
|
ENST00000688411.1:c.808A>T
|
ENSP00000510146.1:n.808A>T
|
|
ENST00000691932.1:c.332A>T
|
ENSP00000509037.1:p.Glu111Val
|
|
ENST00000692637.1:c.16328A>T
|
ENSP00000509666.1:p.Glu5443Val
|
|
ENST00000301067.12:c.16331A>T
MANE Select
|
ENSP00000301067.7:p.Glu5444Val
|
|
ENST00000301067.11:c.16331A>T
|
ENSP00000301067.7:p.Glu5444Val
|
|
ENST00000526209.1:c.374A>T
|
ENSP00000435714.1:p.Glu125Val
|
|
NM_003482.3:c.16331A>T
|
NP_003473.3:p.Glu5444Val
|
|
XM_005269162.3:c.16331A>T
|
XP_005269219.1:p.Glu5444Val
|
|
XM_006719614.2:c.16340A>T
|
XP_006719677.1:p.Glu5447Val
|
|
XM_006719616.2:c.16328A>T
|
XP_006719679.1:p.Glu5443Val
|
|
XM_011538770.1:c.16388A>T
|
XP_011537072.1:p.Glu5463Val
|
|
XM_011538771.1:c.16385A>T
|
XP_011537073.1:p.Glu5462Val
|
|
XM_011538772.1:c.16379A>T
|
XP_011537074.1:p.Glu5460Val
|
|
XM_011538773.1:c.16376A>T
|
XP_011537075.1:p.Glu5459Val
|
|
XM_011538774.1:c.16367A>T
|
XP_011537076.1:p.Glu5456Val
|
|
XM_011538775.1:c.16322A>T
|
XP_011537077.1:p.Glu5441Val
|
|
XM_011538776.1:c.16295A>T
|
XP_011537078.1:p.Glu5432Val
|
|
XM_005269162.4:c.16331A>T
|
XP_005269219.1:p.Glu5444Val
|
|
XM_006719614.4:c.16340A>T
|
XP_006719677.1:p.Glu5447Val
|
|
XM_006719616.3:c.16328A>T
|
XP_006719679.1:p.Glu5443Val
|
|
XM_011538770.2:c.16388A>T
|
XP_011537072.1:p.Glu5463Val
|
|
XM_011538771.2:c.16385A>T
|
XP_011537073.1:p.Glu5462Val
|
|
XM_011538772.2:c.16379A>T
|
XP_011537074.1:p.Glu5460Val
|
|
XM_011538773.2:c.16376A>T
|
XP_011537075.1:p.Glu5459Val
|
|
XM_011538774.2:c.16367A>T
|
XP_011537076.1:p.Glu5456Val
|
|
XM_011538776.2:c.16295A>T
|
XP_011537078.1:p.Glu5432Val
|
|
XR_001748874.1:n.16508A>T
|
|
|
NM_003482.4:c.16331A>T
MANE Select
|
NP_003473.3:p.Glu5444Val
|
|