ENST00000525346.6:c.1156del
|
ENSP00000435707.3:p.Asp386MetfsTer27
|
|
ENST00000526780.6:c.1156del
|
ENSP00000435668.2:p.Asp386MetfsTer27
|
|
ENST00000527316.6:c.982del
|
ENSP00000435047.2:p.Asp328MetfsTer27
|
|
ENST00000682708.1:c.1207del
|
ENSP00000506866.1:p.Asp403MetfsTer27
|
|
ENST00000683287.1:c.1192del
|
ENSP00000507607.1:p.Asp398MetfsTer27
|
|
ENST00000683714.1:c.1164del
|
ENSP00000508207.1:p.Met389TrpfsTer?
|
|
ENST00000684396.1:n.1196del
|
|
|
ENST00000685320.1:c.571del
|
ENSP00000509319.1:p.Asp191MetfsTer27
|
|
ENST00000690257.1:c.1060del
|
ENSP00000510750.1:p.Asp354MetfsTer27
|
|
ENST00000355527.8:c.1156del
MANE Select
|
ENSP00000347717.4:p.Asp386MetfsTer27
|
|
ENST00000355527.7:c.1156del
|
ENSP00000347717.3:p.Asp386MetfsTer27
|
|
ENST00000407721.6:c.1156del
|
ENSP00000384739.2:p.Asp386MetfsTer27
|
|
ENST00000525137.1:c.657del
|
ENSP00000435956.1:p.Met220TrpfsTer?
|
|
ENST00000533800.5:c.406del
|
ENSP00000435011.1:p.Asp136MetfsTer27
|
|
ENST00000534795.5:c.319+2165del
|
|
|
NM_001163817.1:c.1156del
|
NP_001157289.1:p.Asp386MetfsTer27
|
|
NM_001360.2:c.1156del , LRG_340t1:c.1156del
|
NP_001351.2:p.Asp386MetfsTer27
|
|
XM_011544777.1:c.1290del
|
XP_011543079.1:p.Met431TrpfsTer?
|
|
XM_011544777.2:c.1290del
|
XP_011543079.1:p.Met431TrpfsTer?
|
|
NM_001163817.2:c.1156del
|
NP_001157289.1:p.Asp386MetfsTer27
|
|
NM_001360.3:c.1156del
MANE Select
|
NP_001351.2:p.Asp386MetfsTer27
|
|