ENST00000525346.6:c.994C>T
|
ENSP00000435707.3:p.Leu332=
|
|
ENST00000526780.6:c.994C>T
|
ENSP00000435668.2:p.Leu332=
|
|
ENST00000527316.6:c.820C>T
|
ENSP00000435047.2:p.Leu274=
|
|
ENST00000682708.1:c.1045C>T
|
ENSP00000506866.1:p.Leu349=
|
|
ENST00000683287.1:c.1030C>T
|
ENSP00000507607.1:p.Leu344=
|
|
ENST00000683714.1:c.1002C>T
|
ENSP00000508207.1:p.Ser334=
|
|
ENST00000684396.1:n.1034C>T
|
|
|
ENST00000685320.1:c.409C>T
|
ENSP00000509319.1:p.Leu137=
|
|
ENST00000690257.1:c.898C>T
|
ENSP00000510750.1:p.Leu300=
|
|
ENST00000355527.8:c.994C>T
MANE Select
|
ENSP00000347717.4:p.Leu332=
|
|
ENST00000355527.7:c.994C>T
|
ENSP00000347717.3:p.Leu332=
|
|
ENST00000407721.6:c.994C>T
|
ENSP00000384739.2:p.Leu332=
|
|
ENST00000525137.1:c.495C>T
|
ENSP00000435956.1:p.Ser165=
|
|
ENST00000533800.5:c.244C>T
|
ENSP00000435011.1:p.Leu82=
|
|
ENST00000534795.5:c.319+2003C>T
|
|
|
NM_001163817.1:c.994C>T
|
NP_001157289.1:p.Leu332=
|
|
NM_001360.2:c.994C>T , LRG_340t1:c.994C>T
|
NP_001351.2:p.Leu332=
|
|
XM_011544777.1:c.1128C>T
|
XP_011543079.1:p.Ser376=
|
|
XM_011544777.2:c.1128C>T
|
XP_011543079.1:p.Ser376=
|
|
NM_001163817.2:c.994C>T
|
NP_001157289.1:p.Leu332=
|
|
NM_001360.3:c.994C>T
MANE Select
|
NP_001351.2:p.Leu332=
|
|