ENST00000525346.6:c.1119G>A
|
ENSP00000435707.3:p.Arg373=
|
|
ENST00000526780.6:c.1119G>A
|
ENSP00000435668.2:p.Arg373=
|
|
ENST00000527316.6:c.945G>A
|
ENSP00000435047.2:p.Arg315=
|
|
ENST00000682708.1:c.1170G>A
|
ENSP00000506866.1:p.Arg390=
|
|
ENST00000683287.1:c.1155G>A
|
ENSP00000507607.1:p.Arg385=
|
|
ENST00000683714.1:c.1127G>A
|
ENSP00000508207.1:p.Gly376Glu
|
|
ENST00000684396.1:n.1159G>A
|
|
|
ENST00000685320.1:c.534G>A
|
ENSP00000509319.1:p.Arg178=
|
|
ENST00000690257.1:c.1023G>A
|
ENSP00000510750.1:p.Arg341=
|
|
ENST00000355527.8:c.1119G>A
MANE Select
|
ENSP00000347717.4:p.Arg373=
|
|
ENST00000355527.7:c.1119G>A
|
ENSP00000347717.3:p.Arg373=
|
|
ENST00000407721.6:c.1119G>A
|
ENSP00000384739.2:p.Arg373=
|
|
ENST00000525137.1:c.620G>A
|
ENSP00000435956.1:p.Gly207Glu
|
|
ENST00000533800.5:c.369G>A
|
ENSP00000435011.1:p.Arg123=
|
|
ENST00000534795.5:c.319+2128G>A
|
|
|
NM_001163817.1:c.1119G>A
|
NP_001157289.1:p.Arg373=
|
|
NM_001360.2:c.1119G>A , LRG_340t1:c.1119G>A
|
NP_001351.2:p.Arg373=
|
|
XM_011544777.1:c.1253G>A
|
XP_011543079.1:p.Gly418Glu
|
|
XM_011544777.2:c.1253G>A
|
XP_011543079.1:p.Gly418Glu
|
|
NM_001163817.2:c.1119G>A
|
NP_001157289.1:p.Arg373=
|
|
NM_001360.3:c.1119G>A
MANE Select
|
NP_001351.2:p.Arg373=
|
|