ENST00000525346.6:c.1033C>G
|
ENSP00000435707.3:p.Leu345Val
|
|
ENST00000526780.6:c.1033C>G
|
ENSP00000435668.2:p.Leu345Val
|
|
ENST00000527316.6:c.859C>G
|
ENSP00000435047.2:p.Leu287Val
|
|
ENST00000682708.1:c.1084C>G
|
ENSP00000506866.1:p.Leu362Val
|
|
ENST00000683287.1:c.1069C>G
|
ENSP00000507607.1:p.Leu357Val
|
|
ENST00000683714.1:c.1041C>G
|
ENSP00000508207.1:p.Ala347=
|
|
ENST00000684396.1:n.1073C>G
|
|
|
ENST00000685320.1:c.448C>G
|
ENSP00000509319.1:p.Leu150Val
|
|
ENST00000690257.1:c.937C>G
|
ENSP00000510750.1:p.Leu313Val
|
|
ENST00000355527.8:c.1033C>G
MANE Select
|
ENSP00000347717.4:p.Leu345Val
|
|
ENST00000355527.7:c.1033C>G
|
ENSP00000347717.3:p.Leu345Val
|
|
ENST00000407721.6:c.1033C>G
|
ENSP00000384739.2:p.Leu345Val
|
|
ENST00000525137.1:c.534C>G
|
ENSP00000435956.1:p.Ala178=
|
|
ENST00000533800.5:c.283C>G
|
ENSP00000435011.1:p.Leu95Val
|
|
ENST00000534795.5:c.319+2042C>G
|
|
|
NM_001163817.1:c.1033C>G
|
NP_001157289.1:p.Leu345Val
|
|
NM_001360.2:c.1033C>G , LRG_340t1:c.1033C>G
|
NP_001351.2:p.Leu345Val
|
|
XM_011544777.1:c.1167C>G
|
XP_011543079.1:p.Ala389=
|
|
XM_011544777.2:c.1167C>G
|
XP_011543079.1:p.Ala389=
|
|
NM_001163817.2:c.1033C>G
|
NP_001157289.1:p.Leu345Val
|
|
NM_001360.3:c.1033C>G
MANE Select
|
NP_001351.2:p.Leu345Val
|
|