ENST00000525346.6:c.1179G>A
|
ENSP00000435707.3:p.Lys393=
|
|
ENST00000526780.6:c.1179G>A
|
ENSP00000435668.2:p.Lys393=
|
|
ENST00000527316.6:c.1005G>A
|
ENSP00000435047.2:p.Lys335=
|
|
ENST00000682708.1:c.1230G>A
|
ENSP00000506866.1:p.Lys410=
|
|
ENST00000683287.1:c.1215G>A
|
ENSP00000507607.1:p.Lys405=
|
|
ENST00000683714.1:c.1187G>A
|
ENSP00000508207.1:p.Ser396Asn
|
|
ENST00000684396.1:n.1219G>A
|
|
|
ENST00000685320.1:c.594G>A
|
ENSP00000509319.1:p.Lys198=
|
|
ENST00000690257.1:c.1083G>A
|
ENSP00000510750.1:p.Lys361=
|
|
ENST00000355527.8:c.1179G>A
MANE Select
|
ENSP00000347717.4:p.Lys393=
|
|
ENST00000355527.7:c.1179G>A
|
ENSP00000347717.3:p.Lys393=
|
|
ENST00000407721.6:c.1179G>A
|
ENSP00000384739.2:p.Lys393=
|
|
ENST00000525137.1:c.680G>A
|
ENSP00000435956.1:p.Ser227Asn
|
|
ENST00000533800.5:c.429G>A
|
ENSP00000435011.1:p.Lys143=
|
|
ENST00000534795.5:c.319+2188G>A
|
|
|
NM_001163817.1:c.1179G>A
|
NP_001157289.1:p.Lys393=
|
|
NM_001360.2:c.1179G>A , LRG_340t1:c.1179G>A
|
NP_001351.2:p.Lys393=
|
|
XM_011544777.1:c.1313G>A
|
XP_011543079.1:p.Ser438Asn
|
|
XM_011544777.2:c.1313G>A
|
XP_011543079.1:p.Ser438Asn
|
|
NM_001163817.2:c.1179G>A
|
NP_001157289.1:p.Lys393=
|
|
NM_001360.3:c.1179G>A
MANE Select
|
NP_001351.2:p.Lys393=
|
|