ENST00000525346.6:c.1165A>C
|
ENSP00000435707.3:p.Arg389=
|
|
ENST00000526780.6:c.1165A>C
|
ENSP00000435668.2:p.Arg389=
|
|
ENST00000527316.6:c.991A>C
|
ENSP00000435047.2:p.Arg331=
|
|
ENST00000682708.1:c.1216A>C
|
ENSP00000506866.1:p.Arg406=
|
|
ENST00000683287.1:c.1201A>C
|
ENSP00000507607.1:p.Arg401=
|
|
ENST00000683714.1:c.1173A>C
|
ENSP00000508207.1:p.Arg391Ser
|
|
ENST00000684396.1:n.1205A>C
|
|
|
ENST00000685320.1:c.580A>C
|
ENSP00000509319.1:p.Arg194=
|
|
ENST00000690257.1:c.1069A>C
|
ENSP00000510750.1:p.Arg357=
|
|
ENST00000355527.8:c.1165A>C
MANE Select
|
ENSP00000347717.4:p.Arg389=
|
|
ENST00000355527.7:c.1165A>C
|
ENSP00000347717.3:p.Arg389=
|
|
ENST00000407721.6:c.1165A>C
|
ENSP00000384739.2:p.Arg389=
|
|
ENST00000525137.1:c.666A>C
|
ENSP00000435956.1:p.Arg222Ser
|
|
ENST00000533800.5:c.415A>C
|
ENSP00000435011.1:p.Arg139=
|
|
ENST00000534795.5:c.319+2174A>C
|
|
|
NM_001163817.1:c.1165A>C
|
NP_001157289.1:p.Arg389=
|
|
NM_001360.2:c.1165A>C , LRG_340t1:c.1165A>C
|
NP_001351.2:p.Arg389=
|
|
XM_011544777.1:c.1299A>C
|
XP_011543079.1:p.Arg433Ser
|
|
XM_011544777.2:c.1299A>C
|
XP_011543079.1:p.Arg433Ser
|
|
NM_001163817.2:c.1165A>C
|
NP_001157289.1:p.Arg389=
|
|
NM_001360.3:c.1165A>C
MANE Select
|
NP_001351.2:p.Arg389=
|
|