ENST00000369409.9:c.371C>A
|
ENSP00000358417.5:p.Ala124Glu
|
|
ENST00000462324.2:n.454C>A
|
|
|
ENST00000641023.2:c.371C>A
MANE Select
|
ENSP00000493175.1:p.Ala124Glu
|
|
ENST00000641074.1:c.371C>A
|
ENSP00000493446.1:p.Ala124Glu
|
|
ENST00000641115.1:c.371C>A
|
ENSP00000493264.1:p.Ala124Glu
|
|
ENST00000641213.1:c.*24C>A
|
ENSP00000493079.1:n.*24C>A
|
|
ENST00000641247.1:c.*90C>A
|
ENSP00000492955.1:n.*90C>A
|
|
ENST00000641272.1:c.305C>A
|
ENSP00000493432.1:p.Ala102Glu
|
|
ENST00000641314.1:n.356C>A
|
|
|
ENST00000641371.1:c.285C>A
|
ENSP00000493305.1:p.Gly95=
|
|
ENST00000641375.1:c.*207C>A
|
ENSP00000493089.1:n.*207C>A
|
|
ENST00000641491.1:c.*24C>A
|
ENSP00000493187.1:n.*24C>A
|
|
ENST00000641513.1:c.*115C>A
|
ENSP00000493398.1:n.*115C>A
|
|
ENST00000641570.1:c.*90C>A
|
ENSP00000493213.1:n.*90C>A
|
|
ENST00000641573.1:n.459C>A
|
|
|
ENST00000641587.1:c.*82C>A
|
ENSP00000493453.1:n.*82C>A
|
|
ENST00000641597.1:c.371C>A
|
ENSP00000493382.1:p.Ala124Glu
|
|
ENST00000641711.1:n.595C>A
|
|
|
ENST00000641756.1:c.*115C>A
|
ENSP00000493147.1:n.*115C>A
|
|
ENST00000641811.1:c.127C>A
|
|
|
ENST00000641847.1:n.230C>A
|
|
|
ENST00000641891.1:c.*197C>A
|
ENSP00000493288.1:n.*197C>A
|
|
ENST00000641927.1:n.311C>A
|
|
|
ENST00000641947.1:c.371C>A
|
ENSP00000492994.1:p.Ala124Glu
|
|
ENST00000642021.1:n.493C>A
|
|
|
ENST00000642041.1:c.*410C>A
|
ENSP00000493415.1:n.*410C>A
|
|
ENST00000369407.3:c.269C>A
|
ENSP00000358415.3:p.Ala90Glu
|
|
ENST00000369409.8:c.371C>A
|
ENSP00000358417.4:p.Ala124Glu
|
|
ENST00000462324.1:n.639C>A
|
|
|
ENST00000493622.5:n.560C>A
|
|
|
NM_006623.3:c.371C>A
|
NP_006614.2:p.Ala124Glu
|
|
XM_011541226.1:c.593C>A
|
XP_011539528.1:p.Ala198Glu
|
|
XM_011541227.1:c.515C>A
|
XP_011539529.1:p.Ala172Glu
|
|
XM_011541228.1:c.482C>A
|
XP_011539530.1:p.Ala161Glu
|
|
XM_011541229.1:c.308C>A
|
XP_011539531.1:p.Ala103Glu
|
|
XM_011541230.1:c.86C>A
|
XP_011539532.1:p.Ala29Glu
|
|
XM_011541231.1:c.77C>A
|
XP_011539533.1:p.Ala26Glu
|
|
XM_011541226.2:c.593C>A
|
XP_011539528.1:p.Ala198Glu
|
|
XM_011541227.2:c.515C>A
|
XP_011539529.1:p.Ala172Glu
|
|
XM_011541228.2:c.482C>A
|
XP_011539530.1:p.Ala161Glu
|
|
XM_011541231.2:c.77C>A
|
XP_011539533.1:p.Ala26Glu
|
|
XM_024446338.1:c.482C>A
|
XP_024302106.1:p.Ala161Glu
|
|
NM_006623.4:c.371C>A
MANE Select
|
NP_006614.2:p.Ala124Glu
|
|