ENST00000525346.6:c.1158T>G
|
ENSP00000435707.3:p.Asp386Glu
|
|
ENST00000526780.6:c.1158T>G
|
ENSP00000435668.2:p.Asp386Glu
|
|
ENST00000527316.6:c.984T>G
|
ENSP00000435047.2:p.Asp328Glu
|
|
ENST00000682708.1:c.1209T>G
|
ENSP00000506866.1:p.Asp403Glu
|
|
ENST00000683287.1:c.1194T>G
|
ENSP00000507607.1:p.Asp398Glu
|
|
ENST00000683714.1:c.1166T>G
|
ENSP00000508207.1:p.Met389Arg
|
|
ENST00000684396.1:n.1198T>G
|
|
|
ENST00000685320.1:c.573T>G
|
ENSP00000509319.1:p.Asp191Glu
|
|
ENST00000690257.1:c.1062T>G
|
ENSP00000510750.1:p.Asp354Glu
|
|
ENST00000355527.8:c.1158T>G
MANE Select
|
ENSP00000347717.4:p.Asp386Glu
|
|
ENST00000355527.7:c.1158T>G
|
ENSP00000347717.3:p.Asp386Glu
|
|
ENST00000407721.6:c.1158T>G
|
ENSP00000384739.2:p.Asp386Glu
|
|
ENST00000525137.1:c.659T>G
|
ENSP00000435956.1:p.Met220Arg
|
|
ENST00000533800.5:c.408T>G
|
ENSP00000435011.1:p.Asp136Glu
|
|
ENST00000534795.5:c.319+2167T>G
|
|
|
NM_001163817.1:c.1158T>G
|
NP_001157289.1:p.Asp386Glu
|
|
NM_001360.2:c.1158T>G , LRG_340t1:c.1158T>G
|
NP_001351.2:p.Asp386Glu
|
|
XM_011544777.1:c.1292T>G
|
XP_011543079.1:p.Met431Arg
|
|
XM_011544777.2:c.1292T>G
|
XP_011543079.1:p.Met431Arg
|
|
NM_001163817.2:c.1158T>G
|
NP_001157289.1:p.Asp386Glu
|
|
NM_001360.3:c.1158T>G
MANE Select
|
NP_001351.2:p.Asp386Glu
|
|