ENST00000369409.9:c.402G>C
|
ENSP00000358417.5:p.Glu134Asp
|
|
ENST00000462324.2:n.485G>C
|
|
|
ENST00000641023.2:c.402G>C
MANE Select
|
ENSP00000493175.1:p.Glu134Asp
|
|
ENST00000641074.1:c.402G>C
|
ENSP00000493446.1:p.Glu134Asp
|
|
ENST00000641115.1:c.402G>C
|
ENSP00000493264.1:p.Glu134Asp
|
|
ENST00000641213.1:c.*55G>C
|
ENSP00000493079.1:n.*55G>C
|
|
ENST00000641247.1:c.*121G>C
|
ENSP00000492955.1:n.*121G>C
|
|
ENST00000641272.1:c.336G>C
|
ENSP00000493432.1:p.Glu112Asp
|
|
ENST00000641314.1:n.387G>C
|
|
|
ENST00000641371.1:c.316G>C
|
ENSP00000493305.1:p.Ala106Pro
|
|
ENST00000641375.1:c.*238G>C
|
ENSP00000493089.1:n.*238G>C
|
|
ENST00000641491.1:c.*55G>C
|
ENSP00000493187.1:n.*55G>C
|
|
ENST00000641513.1:c.*146G>C
|
ENSP00000493398.1:n.*146G>C
|
|
ENST00000641570.1:c.*121G>C
|
ENSP00000493213.1:n.*121G>C
|
|
ENST00000641573.1:n.490G>C
|
|
|
ENST00000641587.1:c.*113G>C
|
ENSP00000493453.1:n.*113G>C
|
|
ENST00000641597.1:c.402G>C
|
ENSP00000493382.1:p.Glu134Asp
|
|
ENST00000641711.1:n.626G>C
|
|
|
ENST00000641756.1:c.*146G>C
|
ENSP00000493147.1:n.*146G>C
|
|
ENST00000641811.1:c.158G>C
|
|
|
ENST00000641847.1:n.261G>C
|
|
|
ENST00000641891.1:c.*228G>C
|
ENSP00000493288.1:n.*228G>C
|
|
ENST00000641927.1:n.342G>C
|
|
|
ENST00000641947.1:c.402G>C
|
ENSP00000492994.1:p.Glu134Asp
|
|
ENST00000642021.1:n.524G>C
|
|
|
ENST00000642041.1:c.*441G>C
|
ENSP00000493415.1:n.*441G>C
|
|
ENST00000369407.3:c.300G>C
|
ENSP00000358415.3:p.Glu100Asp
|
|
ENST00000369409.8:c.402G>C
|
ENSP00000358417.4:p.Glu134Asp
|
|
ENST00000462324.1:n.670G>C
|
|
|
ENST00000493622.5:n.591G>C
|
|
|
NM_006623.3:c.402G>C
|
NP_006614.2:p.Glu134Asp
|
|
XM_011541226.1:c.624G>C
|
XP_011539528.1:p.Glu208Asp
|
|
XM_011541227.1:c.546G>C
|
XP_011539529.1:p.Glu182Asp
|
|
XM_011541228.1:c.513G>C
|
XP_011539530.1:p.Glu171Asp
|
|
XM_011541229.1:c.339G>C
|
XP_011539531.1:p.Glu113Asp
|
|
XM_011541230.1:c.117G>C
|
XP_011539532.1:p.Glu39Asp
|
|
XM_011541231.1:c.108G>C
|
XP_011539533.1:p.Glu36Asp
|
|
XM_011541226.2:c.624G>C
|
XP_011539528.1:p.Glu208Asp
|
|
XM_011541227.2:c.546G>C
|
XP_011539529.1:p.Glu182Asp
|
|
XM_011541228.2:c.513G>C
|
XP_011539530.1:p.Glu171Asp
|
|
XM_011541231.2:c.108G>C
|
XP_011539533.1:p.Glu36Asp
|
|
XM_024446338.1:c.513G>C
|
XP_024302106.1:p.Glu171Asp
|
|
NM_006623.4:c.402G>C
MANE Select
|
NP_006614.2:p.Glu134Asp
|
|