ENST00000369409.9:c.359A>G
|
ENSP00000358417.5:p.Gln120Arg
|
|
ENST00000462324.2:n.442A>G
|
|
|
ENST00000641023.2:c.359A>G
MANE Select
|
ENSP00000493175.1:p.Gln120Arg
|
|
ENST00000641074.1:c.359A>G
|
ENSP00000493446.1:p.Gln120Arg
|
|
ENST00000641115.1:c.359A>G
|
ENSP00000493264.1:p.Gln120Arg
|
|
ENST00000641213.1:c.*12A>G
|
ENSP00000493079.1:n.*12A>G
|
|
ENST00000641247.1:c.*78A>G
|
ENSP00000492955.1:n.*78A>G
|
|
ENST00000641272.1:c.293A>G
|
ENSP00000493432.1:p.Gln98Arg
|
|
ENST00000641314.1:n.344A>G
|
|
|
ENST00000641371.1:c.273A>G
|
ENSP00000493305.1:p.Ala91=
|
|
ENST00000641375.1:c.*195A>G
|
ENSP00000493089.1:n.*195A>G
|
|
ENST00000641491.1:c.*12A>G
|
ENSP00000493187.1:n.*12A>G
|
|
ENST00000641513.1:c.*103A>G
|
ENSP00000493398.1:n.*103A>G
|
|
ENST00000641570.1:c.*78A>G
|
ENSP00000493213.1:n.*78A>G
|
|
ENST00000641573.1:n.447A>G
|
|
|
ENST00000641587.1:c.*70A>G
|
ENSP00000493453.1:n.*70A>G
|
|
ENST00000641597.1:c.359A>G
|
ENSP00000493382.1:p.Gln120Arg
|
|
ENST00000641711.1:n.583A>G
|
|
|
ENST00000641756.1:c.*103A>G
|
ENSP00000493147.1:n.*103A>G
|
|
ENST00000641811.1:c.115A>G
|
|
|
ENST00000641847.1:n.218A>G
|
|
|
ENST00000641891.1:c.*185A>G
|
ENSP00000493288.1:n.*185A>G
|
|
ENST00000641927.1:n.299A>G
|
|
|
ENST00000641947.1:c.359A>G
|
ENSP00000492994.1:p.Gln120Arg
|
|
ENST00000642021.1:n.481A>G
|
|
|
ENST00000642041.1:c.*398A>G
|
ENSP00000493415.1:n.*398A>G
|
|
ENST00000369407.3:c.257A>G
|
ENSP00000358415.3:p.Gln86Arg
|
|
ENST00000369409.8:c.359A>G
|
ENSP00000358417.4:p.Gln120Arg
|
|
ENST00000462324.1:n.627A>G
|
|
|
ENST00000493622.5:n.548A>G
|
|
|
NM_006623.3:c.359A>G
|
NP_006614.2:p.Gln120Arg
|
|
XM_011541226.1:c.581A>G
|
XP_011539528.1:p.Gln194Arg
|
|
XM_011541227.1:c.503A>G
|
XP_011539529.1:p.Gln168Arg
|
|
XM_011541228.1:c.470A>G
|
XP_011539530.1:p.Gln157Arg
|
|
XM_011541229.1:c.296A>G
|
XP_011539531.1:p.Gln99Arg
|
|
XM_011541230.1:c.74A>G
|
XP_011539532.1:p.Gln25Arg
|
|
XM_011541231.1:c.65A>G
|
XP_011539533.1:p.Gln22Arg
|
|
XM_011541226.2:c.581A>G
|
XP_011539528.1:p.Gln194Arg
|
|
XM_011541227.2:c.503A>G
|
XP_011539529.1:p.Gln168Arg
|
|
XM_011541228.2:c.470A>G
|
XP_011539530.1:p.Gln157Arg
|
|
XM_011541231.2:c.65A>G
|
XP_011539533.1:p.Gln22Arg
|
|
XM_024446338.1:c.470A>G
|
XP_024302106.1:p.Gln157Arg
|
|
NM_006623.4:c.359A>G
MANE Select
|
NP_006614.2:p.Gln120Arg
|
|