ENST00000525346.6:c.984C=
|
ENSP00000435707.3:p.His328=
|
|
ENST00000526780.6:c.984C=
|
ENSP00000435668.2:p.His328=
|
|
ENST00000527316.6:c.810C=
|
ENSP00000435047.2:p.His270=
|
|
ENST00000682708.1:c.1035C=
|
ENSP00000506866.1:p.His345=
|
|
ENST00000683287.1:c.1020C=
|
ENSP00000507607.1:p.His340=
|
|
ENST00000683714.1:c.992C=
|
ENSP00000508207.1:p.Thr331=
|
|
ENST00000684396.1:n.1024C=
|
|
|
ENST00000685320.1:c.399C=
|
ENSP00000509319.1:p.His133=
|
|
ENST00000690257.1:c.888C=
|
ENSP00000510750.1:p.His296=
|
|
ENST00000355527.8:c.984C=
MANE Select
|
ENSP00000347717.4:p.His328=
|
|
ENST00000355527.7:c.984C=
|
ENSP00000347717.3:p.His328=
|
|
ENST00000407721.6:c.984C=
|
ENSP00000384739.2:p.His328=
|
|
ENST00000525137.1:c.485C=
|
ENSP00000435956.1:p.Thr162=
|
|
ENST00000533800.5:c.234C=
|
ENSP00000435011.1:p.His78=
|
|
ENST00000534795.5:c.319+1993C=
|
|
|
NM_001163817.1:c.984C=
|
NP_001157289.1:p.His328=
|
|
NM_001360.2:c.984C= , LRG_340t1:c.984C=
|
NP_001351.2:p.His328=
|
|
XM_011544777.1:c.1118C=
|
XP_011543079.1:p.Thr373=
|
|
XM_011544777.2:c.1118C=
|
XP_011543079.1:p.Thr373=
|
|
NM_001163817.2:c.984C=
|
NP_001157289.1:p.His328=
|
|
NM_001360.3:c.984C=
MANE Select
|
NP_001351.2:p.His328=
|
|