ENST00000682153.1:c.9954A>T
|
ENSP00000507923.1:p.Glu3318Asp
|
|
ENST00000682358.1:n.10024A>T
|
|
|
ENST00000683334.1:c.*5636A>T
|
ENSP00000507369.1:n.*5636A>T
|
|
ENST00000357162.7:c.9879A>T
MANE Select
|
ENSP00000349685.2:p.Glu3293Asp
|
|
ENST00000358544.7:c.9954A>T
MANE Plus Clinical
|
ENSP00000351346.2:p.Glu3318Asp
|
|
ENST00000357162.6:c.9879A>T
|
ENSP00000349685.2:p.Glu3293Asp
|
|
ENST00000358544.6:c.9954A>T
|
ENSP00000351346.2:p.Glu3318Asp
|
|
NM_017890.4:c.9954A>T , LRG_351t1:c.9954A>T
|
NP_060360.3:p.Glu3318Asp
|
|
NM_152564.4:c.9879A>T , LRG_351t2:c.9879A>T
|
NP_689777.3:p.Glu3293Asp
|
|
XM_005250800.2:c.9954A>T
|
XP_005250857.1:p.Glu3318Asp
|
|
XM_005250801.3:c.9954A>T
|
XP_005250858.1:p.Glu3318Asp
|
|
XM_011516848.1:c.9951A>T
|
XP_011515150.1:p.Glu3317Asp
|
|
XM_011516849.1:c.9876A>T
|
XP_011515151.1:p.Glu3292Asp
|
|
XM_011516850.1:c.9576A>T
|
XP_011515152.1:p.Glu3192Asp
|
|
XM_011516851.1:c.6840A>T
|
XP_011515153.1:p.Glu2280Asp
|
|
XM_011516852.1:c.6840A>T
|
XP_011515154.1:p.Glu2280Asp
|
|
XM_011516854.1:c.5733A>T
|
XP_011515156.1:p.Glu1911Asp
|
|
XM_005250800.3:c.9954A>T
|
XP_005250857.1:p.Glu3318Asp
|
|
XM_005250801.5:c.9954A>T
|
XP_005250858.1:p.Glu3318Asp
|
|
XM_011516848.2:c.9951A>T
|
XP_011515150.1:p.Glu3317Asp
|
|
XM_011516849.2:c.9876A>T
|
XP_011515151.1:p.Glu3292Asp
|
|
XM_011516850.2:c.9576A>T
|
XP_011515152.1:p.Glu3192Asp
|
|
XM_011516851.2:c.6840A>T
|
XP_011515153.1:p.Glu2280Asp
|
|
XM_011516852.2:c.6840A>T
|
XP_011515154.1:p.Glu2280Asp
|
|
XM_011516854.2:c.5733A>T
|
XP_011515156.1:p.Glu1911Asp
|
|
XM_017013109.1:c.9759A>T
|
XP_016868598.1:p.Glu3253Asp
|
|
XM_017013111.1:c.6840A>T
|
XP_016868600.1:p.Glu2280Asp
|
|
XM_017013112.1:c.5511A>T
|
XP_016868601.1:p.Glu1837Asp
|
|
XM_024447074.1:c.8739A>T
|
XP_024302842.1:p.Glu2913Asp
|
|
NM_017890.5:c.9954A>T
MANE Plus Clinical
|
NP_060360.3:p.Glu3318Asp
|
|
NM_152564.5:c.9879A>T
MANE Select
|
NP_689777.3:p.Glu3293Asp
|
|