ENST00000373327.5:c.1745A>T
MANE Select
|
ENSP00000362424.4:p.Glu582Val
|
|
ENST00000373327.4:c.1745A>T
|
ENSP00000362424.4:p.Glu582Val
|
|
ENST00000391993.7:c.1547A>T
|
ENSP00000375851.3:p.Glu516Val
|
|
ENST00000462122.1:n.756A>T
|
|
|
ENST00000483951.1:n.93A>T
|
|
|
NM_001139490.1:c.1547A>T
|
NP_001132962.1:p.Glu516Val
|
|
NM_015650.3:c.1745A>T
|
NP_056465.2:p.Glu582Val
|
|
XM_006712414.1:c.1544A>T
|
XP_006712477.1:p.Glu515Val
|
|
XM_011510944.1:c.1847A>T
|
XP_011509246.1:p.Glu616Val
|
|
XM_011510945.1:c.1808A>T
|
XP_011509247.1:p.Glu603Val
|
|
XM_011510946.1:c.1775A>T
|
XP_011509248.1:p.Glu592Val
|
|
XM_011510947.1:c.1715A>T
|
XP_011509249.1:p.Glu572Val
|
|
XM_011510948.1:c.1649A>T
|
XP_011509250.1:p.Glu550Val
|
|
XM_011510950.1:c.713A>T
|
XP_011509252.1:p.Glu238Val
|
|
XR_922902.1:n.2044A>T
|
|
|
XM_006712414.2:c.1544A>T
|
XP_006712477.1:p.Glu515Val
|
|
XM_011510944.2:c.1847A>T
|
XP_011509246.1:p.Glu616Val
|
|
XM_011510945.2:c.1808A>T
|
XP_011509247.1:p.Glu603Val
|
|
XM_011510946.2:c.1775A>T
|
XP_011509248.1:p.Glu592Val
|
|
XM_011510947.2:c.1715A>T
|
XP_011509249.1:p.Glu572Val
|
|
XM_011510948.2:c.1649A>T
|
XP_011509250.1:p.Glu550Val
|
|
XM_011510950.2:c.713A>T
|
XP_011509252.1:p.Glu238Val
|
|
XM_017003789.1:c.1844A>T
|
XP_016859278.1:p.Glu615Val
|
|
XR_001738696.1:n.1573A>T
|
|
|
XR_001738697.1:n.1570A>T
|
|
|
XR_922902.2:n.2107A>T
|
|
|
NM_015650.4:c.1745A>T
MANE Select
|
NP_056465.2:p.Glu582Val
|
|