ENST00000369409.9:c.461G=
|
ENSP00000358417.5:p.Gly154=
|
|
ENST00000462324.2:n.544G=
|
|
|
ENST00000641023.2:c.461G=
MANE Select
|
ENSP00000493175.1:p.Gly154=
|
|
ENST00000641074.1:c.461G=
|
ENSP00000493446.1:p.Gly154=
|
|
ENST00000641115.1:c.461G=
|
ENSP00000493264.1:p.Gly154=
|
|
ENST00000641213.1:c.*114G=
|
ENSP00000493079.1:n.*114G=
|
|
ENST00000641247.1:c.*180G=
|
ENSP00000492955.1:n.*180G=
|
|
ENST00000641272.1:c.395G=
|
ENSP00000493432.1:p.Gly132=
|
|
ENST00000641314.1:n.446G=
|
|
|
ENST00000641371.1:c.375G=
|
ENSP00000493305.1:p.Gly125=
|
|
ENST00000641375.1:c.*297G=
|
ENSP00000493089.1:n.*297G=
|
|
ENST00000641455.1:n.6G=
|
|
|
ENST00000641491.1:c.*114G=
|
ENSP00000493187.1:n.*114G=
|
|
ENST00000641570.1:c.*180G=
|
ENSP00000493213.1:n.*180G=
|
|
ENST00000641573.1:n.549G=
|
|
|
ENST00000641587.1:c.*172G=
|
ENSP00000493453.1:n.*172G=
|
|
ENST00000641597.1:c.461G=
|
ENSP00000493382.1:p.Gly154=
|
|
ENST00000641711.1:n.685G=
|
|
|
ENST00000641756.1:c.*205G=
|
ENSP00000493147.1:n.*205G=
|
|
ENST00000641811.1:c.217G=
|
|
|
ENST00000641847.1:n.320G=
|
|
|
ENST00000641891.1:c.*287G=
|
ENSP00000493288.1:n.*287G=
|
|
ENST00000641927.1:n.401G=
|
|
|
ENST00000641947.1:c.461G=
|
ENSP00000492994.1:p.Gly154=
|
|
ENST00000642021.1:n.583G=
|
|
|
ENST00000642041.1:c.*500G=
|
ENSP00000493415.1:n.*500G=
|
|
ENST00000369407.3:c.359G=
|
ENSP00000358415.3:p.Gly120=
|
|
ENST00000369409.8:c.461G=
|
ENSP00000358417.4:p.Gly154=
|
|
ENST00000462324.1:n.729G=
|
|
|
ENST00000493622.5:n.650G=
|
|
|
NM_006623.3:c.461G=
|
NP_006614.2:p.Gly154=
|
|
XM_011541226.1:c.683G=
|
XP_011539528.1:p.Gly228=
|
|
XM_011541227.1:c.605G=
|
XP_011539529.1:p.Gly202=
|
|
XM_011541228.1:c.572G=
|
XP_011539530.1:p.Gly191=
|
|
XM_011541229.1:c.398G=
|
XP_011539531.1:p.Gly133=
|
|
XM_011541230.1:c.176G=
|
XP_011539532.1:p.Gly59=
|
|
XM_011541231.1:c.167G=
|
XP_011539533.1:p.Gly56=
|
|
XM_011541226.2:c.683G=
|
XP_011539528.1:p.Gly228=
|
|
XM_011541227.2:c.605G=
|
XP_011539529.1:p.Gly202=
|
|
XM_011541228.2:c.572G=
|
XP_011539530.1:p.Gly191=
|
|
XM_011541231.2:c.167G=
|
XP_011539533.1:p.Gly56=
|
|
XM_024446338.1:c.572G=
|
XP_024302106.1:p.Gly191=
|
|
NM_006623.4:c.461G=
MANE Select
|
NP_006614.2:p.Gly154=
|
|