ENST00000381733.9:c.807T>G
|
ENSP00000371152.4:p.Thr269=
|
|
ENST00000517409.2:n.727T>G
|
|
|
ENST00000518746.2:n.2445T>G
|
|
|
ENST00000520781.6:c.684T>G
|
ENSP00000427751.1:p.Thr228=
|
|
ENST00000521542.2:n.67T>G
|
|
|
ENST00000635756.1:c.172T>G
|
|
|
ENST00000635944.1:c.*595T>G
|
ENSP00000490195.1:n.*595T>G
|
|
ENST00000635998.1:c.759T>G
|
ENSP00000490506.1:p.Thr253=
|
|
ENST00000636009.1:c.616T>G
|
ENSP00000489988.1:n.616T>G
|
|
ENST00000636033.1:c.*595T>G
|
ENSP00000489617.1:n.*595T>G
|
|
ENST00000636050.1:c.*602T>G
|
ENSP00000490562.1:n.*602T>G
|
|
ENST00000636128.1:c.438T>G
|
ENSP00000489789.1:p.Thr146=
|
|
ENST00000636160.1:c.*651T>G
|
ENSP00000489651.1:n.*651T>G
|
|
ENST00000636171.1:c.702T>G
|
ENSP00000489761.1:p.Thr234=
|
|
ENST00000636455.1:c.807T>G
|
ENSP00000490502.1:p.Thr269=
|
|
ENST00000636494.1:c.*539T>G
|
ENSP00000490388.1:n.*539T>G
|
|
ENST00000636563.1:n.421T>G
|
|
|
ENST00000636577.1:c.699T>G
|
ENSP00000490027.1:p.Thr233=
|
|
ENST00000636691.1:c.564T>G
|
ENSP00000490725.1:p.Thr188=
|
|
ENST00000636701.1:c.*410T>G
|
ENSP00000489800.1:n.*410T>G
|
|
ENST00000636815.1:c.676T>G
|
|
|
ENST00000636920.1:c.*595T>G
|
ENSP00000490437.1:n.*595T>G
|
|
ENST00000636997.1:c.672T>G
|
ENSP00000490093.1:p.Thr224=
|
|
ENST00000637013.1:c.*1127T>G
|
ENSP00000490596.1:n.*1127T>G
|
|
ENST00000637014.1:n.1166T>G
|
|
|
ENST00000637095.1:c.*539T>G
|
ENSP00000490415.1:n.*539T>G
|
|
ENST00000637244.1:c.*1277T>G
|
ENSP00000490188.1:n.*1277T>G
|
|
ENST00000637343.1:n.2196T>G
|
|
|
ENST00000637429.1:c.*971T>G
|
ENSP00000490522.1:n.*971T>G
|
|
ENST00000637484.1:c.*721T>G
|
ENSP00000490837.1:n.*721T>G
|
|
ENST00000637528.1:c.696T>G
|
ENSP00000490801.1:p.Thr232=
|
|
ENST00000637609.1:n.3480T>G
|
|
|
ENST00000637636.1:c.753T>G
|
ENSP00000490112.1:p.Thr251=
|
|
ENST00000637790.2:c.759T>G
MANE Select
|
ENSP00000490272.1:p.Thr253=
|
|
ENST00000637857.1:n.1125T>G
|
|
|
ENST00000637922.1:c.564T>G
|
ENSP00000490071.1:p.Thr188=
|
|
ENST00000637991.1:c.732T>G
|
ENSP00000489901.1:p.Thr244=
|
|
ENST00000638028.1:n.976T>G
|
|
|
ENST00000638069.1:n.1580T>G
|
|
|
ENST00000262097.10:c.759T>G
|
ENSP00000262097.6:p.Thr253=
|
|
ENST00000314146.10:c.741T>G
|
ENSP00000326970.10:p.Thr247=
|
|
ENST00000381733.8:c.807T>G
|
ENSP00000371152.4:p.Thr269=
|
|
ENST00000518746.1:n.576T>G
|
|
|
ENST00000519468.5:n.588T>G
|
|
|
ENST00000520781.5:c.684T>G
|
ENSP00000427751.1:p.Thr228=
|
|
ENST00000521542.1:n.472T>G
|
|
|
NM_001127505.1:c.741T>G
|
NP_001120977.1:p.Thr247=
|
|
NM_001127505.2:c.741T>G
|
NP_001120977.1:p.Thr247=
|
|
NM_004315.4:c.807T>G
|
NP_004306.3:p.Thr269=
|
|
NM_004315.5:c.807T>G
|
NP_004306.3:p.Thr269=
|
|
NM_177924.3:c.759T>G
|
NP_808592.2:p.Thr253=
|
|
NM_177924.4:c.759T>G
|
NP_808592.2:p.Thr253=
|
|
XM_005273504.2:c.693T>G
|
XP_005273561.1:p.Thr231=
|
|
NM_001363743.1:c.564T>G
|
NP_001350672.1:p.Thr188=
|
|
XM_005273504.3:c.693T>G
|
XP_005273561.1:p.Thr231=
|
|
NM_177924.5:c.759T>G
MANE Select
|
NP_808592.2:p.Thr253=
|
|
NM_001127505.3:c.741T>G
|
NP_001120977.1:p.Thr247=
|
|
NM_001363743.2:c.564T>G
|
NP_001350672.1:p.Thr188=
|
|
NM_004315.6:c.807T>G
|
NP_004306.3:p.Thr269=
|
|