ENST00000525346.6:c.1174A=
|
ENSP00000435707.3:p.Ser392=
|
|
ENST00000526780.6:c.1174A=
|
ENSP00000435668.2:p.Ser392=
|
|
ENST00000527316.6:c.1000A=
|
ENSP00000435047.2:p.Ser334=
|
|
ENST00000682708.1:c.1225A=
|
ENSP00000506866.1:p.Ser409=
|
|
ENST00000683287.1:c.1210A=
|
ENSP00000507607.1:p.Ser404=
|
|
ENST00000683714.1:c.1182A=
|
ENSP00000508207.1:p.Thr394=
|
|
ENST00000684396.1:n.1214A=
|
|
|
ENST00000685320.1:c.589A=
|
ENSP00000509319.1:p.Ser197=
|
|
ENST00000690257.1:c.1078A=
|
ENSP00000510750.1:p.Ser360=
|
|
ENST00000355527.8:c.1174A=
MANE Select
|
ENSP00000347717.4:p.Ser392=
|
|
ENST00000355527.7:c.1174A=
|
ENSP00000347717.3:p.Ser392=
|
|
ENST00000407721.6:c.1174A=
|
ENSP00000384739.2:p.Ser392=
|
|
ENST00000525137.1:c.675A=
|
ENSP00000435956.1:p.Thr225=
|
|
ENST00000533800.5:c.424A=
|
ENSP00000435011.1:p.Ser142=
|
|
ENST00000534795.5:c.319+2183A=
|
|
|
NM_001163817.1:c.1174A=
|
NP_001157289.1:p.Ser392=
|
|
NM_001360.2:c.1174A= , LRG_340t1:c.1174A=
|
NP_001351.2:p.Ser392=
|
|
XM_011544777.1:c.1308A=
|
XP_011543079.1:p.Thr436=
|
|
XM_011544777.2:c.1308A=
|
XP_011543079.1:p.Thr436=
|
|
NM_001163817.2:c.1174A=
|
NP_001157289.1:p.Ser392=
|
|
NM_001360.3:c.1174A=
MANE Select
|
NP_001351.2:p.Ser392=
|
|