ENST00000405460.9:c.11501A>T
MANE Select
|
ENSP00000384582.2:p.Glu3834Val
|
|
ENST00000425867.3:c.632A>T
|
ENSP00000392618.3:p.Glu211Val
|
|
ENST00000639431.1:c.265+78897A>T
|
ENSP00000491057.1:n.265+78897A>T
|
|
ENST00000640374.1:n.4645A>T
|
|
|
ENST00000640464.1:n.1920A>T
|
|
|
ENST00000405460.6:c.11501A>T
|
ENSP00000384582.2:p.Glu3834Val
|
|
ENST00000509621.1:c.4198A>T
|
|
|
NM_032119.3:c.11501A>T
|
NP_115495.3:p.Glu3834Val
|
|
NR_003149.1:n.11514A>T
|
|
|
XM_011543675.1:c.11498A>T
|
XP_011541977.1:p.Glu3833Val
|
|
XM_011543676.1:c.11420A>T
|
XP_011541978.1:p.Glu3807Val
|
|
XM_011543677.1:c.8804A>T
|
XP_011541979.1:p.Glu2935Val
|
|
XM_011543678.1:c.11501A>T
|
XP_011541980.1:p.Glu3834Val
|
|
NM_032119.4:c.11501A>T
MANE Select
|
NP_115495.3:p.Glu3834Val
|
|
XM_017009963.2:c.11522A>T
|
XP_016865452.1:p.Glu3841Val
|
|
XM_017009964.2:c.11519A>T
|
XP_016865453.1:p.Glu3840Val
|
|
XM_017009965.1:c.11519A>T
|
XP_016865454.1:p.Glu3840Val
|
|
XM_017009966.2:c.11441A>T
|
XP_016865455.1:p.Glu3814Val
|
|
XM_017009967.1:c.11426A>T
|
XP_016865456.1:p.Glu3809Val
|
|
XM_017009968.2:c.11522A>T
|
XP_016865457.1:p.Glu3841Val
|
|
XM_017009969.2:c.11522A>T
|
XP_016865458.1:p.Glu3841Val
|
|
XM_017009970.2:c.11522A>T
|
XP_016865459.1:p.Glu3841Val
|
|
XM_017009971.2:c.11522A>T
|
XP_016865460.1:p.Glu3841Val
|
|
XM_017009972.1:c.4640A>T
|
XP_016865461.1:p.Glu1547Val
|
|
XM_017009973.1:c.4619A>T
|
XP_016865462.1:p.Glu1540Val
|
|
NR_003149.2:n.11517A>T
|
|
|