ENST00000366577.10:c.1775A>T
MANE Select
|
ENSP00000355536.5:p.Glu592Val
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ENST00000535889.6:c.1775A>T
|
ENSP00000441845.1:p.Glu592Val
|
|
ENST00000650888.1:c.*817A>T
|
ENSP00000498393.1:n.*817A>T
|
|
ENST00000651455.1:c.*519A>T
|
ENSP00000498963.1:n.*519A>T
|
|
ENST00000674797.2:c.1427A>T
|
ENSP00000502299.2:p.Glu476Val
|
|
ENST00000679569.1:n.2089A>T
|
|
|
ENST00000679842.1:c.1775A>T
|
ENSP00000506109.1:p.Glu592Val
|
|
ENST00000680454.1:n.2219A>T
|
|
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ENST00000681102.1:c.1595A>T
|
ENSP00000505600.1:p.Glu532Val
|
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ENST00000681177.1:c.1516-7233A>T
|
ENSP00000506327.1:n.1516-7233A>T
|
|
ENST00000681937.1:n.2148-7233A>T
|
|
|
ENST00000366576.3:c.437A>T
|
ENSP00000355535.3:p.Glu146Val
|
|
ENST00000366577.9:c.1775A>T
|
ENSP00000355536.5:p.Glu592Val
|
|
ENST00000463959.1:n.1794A>T
|
|
|
ENST00000535889.5:c.1775A>T
|
ENSP00000441845.1:p.Glu592Val
|
|
NM_000254.2:c.1775A>T
|
NP_000245.2:p.Glu592Val
|
|
NM_001291939.1:c.1775A>T
|
NP_001278868.1:p.Glu592Val
|
|
NM_001291940.1:c.554A>T
|
NP_001278869.1:p.Glu185Val
|
|
XM_005273141.3:c.1772A>T
|
XP_005273198.1:p.Glu591Val
|
|
XM_006711769.2:c.1775A>T
|
XP_006711832.1:p.Glu592Val
|
|
XM_006711770.1:c.839A>T
|
XP_006711833.1:p.Glu280Val
|
|
XM_011544193.1:c.1775A>T
|
XP_011542495.1:p.Glu592Val
|
|
XM_011544194.1:c.1943A>T
|
XP_011542496.1:p.Glu648Val
|
|
XM_005273141.5:c.1772A>T
|
XP_005273198.1:p.Glu591Val
|
|
XM_006711770.3:c.839A>T
|
XP_006711833.1:p.Glu280Val
|
|
XM_011544194.3:c.1943A>T
|
XP_011542496.1:p.Glu648Val
|
|
XM_017001329.2:c.1943A>T
|
XP_016856818.1:p.Glu648Val
|
|
XM_017001330.2:c.1943A>T
|
XP_016856819.1:p.Glu648Val
|
|
NM_001291940.2:c.554A>T
|
NP_001278869.1:p.Glu185Val
|
|
NM_000254.3:c.1775A>T
MANE Select
|
NP_000245.2:p.Glu592Val
|
|