ENST00000525346.6:c.1029G>C
|
ENSP00000435707.3:p.Leu343=
|
|
ENST00000526780.6:c.1029G>C
|
ENSP00000435668.2:p.Leu343=
|
|
ENST00000527316.6:c.855G>C
|
ENSP00000435047.2:p.Leu285=
|
|
ENST00000682708.1:c.1080G>C
|
ENSP00000506866.1:p.Leu360=
|
|
ENST00000683287.1:c.1065G>C
|
ENSP00000507607.1:p.Leu355=
|
|
ENST00000683714.1:c.1037G>C
|
ENSP00000508207.1:p.Trp346Ser
|
|
ENST00000684396.1:n.1069G>C
|
|
|
ENST00000685320.1:c.444G>C
|
ENSP00000509319.1:p.Leu148=
|
|
ENST00000690257.1:c.933G>C
|
ENSP00000510750.1:p.Leu311=
|
|
ENST00000355527.8:c.1029G>C
MANE Select
|
ENSP00000347717.4:p.Leu343=
|
|
ENST00000355527.7:c.1029G>C
|
ENSP00000347717.3:p.Leu343=
|
|
ENST00000407721.6:c.1029G>C
|
ENSP00000384739.2:p.Leu343=
|
|
ENST00000525137.1:c.530G>C
|
ENSP00000435956.1:p.Trp177Ser
|
|
ENST00000533800.5:c.279G>C
|
ENSP00000435011.1:p.Leu93=
|
|
ENST00000534795.5:c.319+2038G>C
|
|
|
NM_001163817.1:c.1029G>C
|
NP_001157289.1:p.Leu343=
|
|
NM_001360.2:c.1029G>C , LRG_340t1:c.1029G>C
|
NP_001351.2:p.Leu343=
|
|
XM_011544777.1:c.1163G>C
|
XP_011543079.1:p.Trp388Ser
|
|
XM_011544777.2:c.1163G>C
|
XP_011543079.1:p.Trp388Ser
|
|
NM_001163817.2:c.1029G>C
|
NP_001157289.1:p.Leu343=
|
|
NM_001360.3:c.1029G>C
MANE Select
|
NP_001351.2:p.Leu343=
|
|