ENST00000525346.6:c.1084C>T
|
ENSP00000435707.3:p.Arg362Cys
|
|
ENST00000526780.6:c.1084C>T
|
ENSP00000435668.2:p.Arg362Cys
|
|
ENST00000527316.6:c.910C>T
|
ENSP00000435047.2:p.Arg304Cys
|
|
ENST00000682708.1:c.1135C>T
|
ENSP00000506866.1:p.Arg379Cys
|
|
ENST00000683287.1:c.1120C>T
|
ENSP00000507607.1:p.Arg374Cys
|
|
ENST00000683714.1:c.1092C>T
|
ENSP00000508207.1:p.Ser364=
|
|
ENST00000684396.1:n.1124C>T
|
|
|
ENST00000685320.1:c.499C>T
|
ENSP00000509319.1:p.Arg167Cys
|
|
ENST00000690257.1:c.988C>T
|
ENSP00000510750.1:p.Arg330Cys
|
|
ENST00000355527.8:c.1084C>T
MANE Select
|
ENSP00000347717.4:p.Arg362Cys
|
|
ENST00000355527.7:c.1084C>T
|
ENSP00000347717.3:p.Arg362Cys
|
|
ENST00000407721.6:c.1084C>T
|
ENSP00000384739.2:p.Arg362Cys
|
|
ENST00000525137.1:c.585C>T
|
ENSP00000435956.1:p.Ser195=
|
|
ENST00000533800.5:c.334C>T
|
ENSP00000435011.1:p.Arg112Cys
|
|
ENST00000534795.5:c.319+2093C>T
|
|
|
NM_001163817.1:c.1084C>T
|
NP_001157289.1:p.Arg362Cys
|
|
NM_001360.2:c.1084C>T , LRG_340t1:c.1084C>T
|
NP_001351.2:p.Arg362Cys
|
|
XM_011544777.1:c.1218C>T
|
XP_011543079.1:p.Ser406=
|
|
XM_011544777.2:c.1218C>T
|
XP_011543079.1:p.Ser406=
|
|
NM_001163817.2:c.1084C>T
|
NP_001157289.1:p.Arg362Cys
|
|
NM_001360.3:c.1084C>T
MANE Select
|
NP_001351.2:p.Arg362Cys
|
|