ENST00000525346.6:c.1027C>G
|
ENSP00000435707.3:p.Leu343Val
|
|
ENST00000526780.6:c.1027C>G
|
ENSP00000435668.2:p.Leu343Val
|
|
ENST00000527316.6:c.853C>G
|
ENSP00000435047.2:p.Leu285Val
|
|
ENST00000682708.1:c.1078C>G
|
ENSP00000506866.1:p.Leu360Val
|
|
ENST00000683287.1:c.1063C>G
|
ENSP00000507607.1:p.Leu355Val
|
|
ENST00000683714.1:c.1035C>G
|
ENSP00000508207.1:p.Cys345Trp
|
|
ENST00000684396.1:n.1067C>G
|
|
|
ENST00000685320.1:c.442C>G
|
ENSP00000509319.1:p.Leu148Val
|
|
ENST00000690257.1:c.931C>G
|
ENSP00000510750.1:p.Leu311Val
|
|
ENST00000355527.8:c.1027C>G
MANE Select
|
ENSP00000347717.4:p.Leu343Val
|
|
ENST00000355527.7:c.1027C>G
|
ENSP00000347717.3:p.Leu343Val
|
|
ENST00000407721.6:c.1027C>G
|
ENSP00000384739.2:p.Leu343Val
|
|
ENST00000525137.1:c.528C>G
|
ENSP00000435956.1:p.Cys176Trp
|
|
ENST00000533800.5:c.277C>G
|
ENSP00000435011.1:p.Leu93Val
|
|
ENST00000534795.5:c.319+2036C>G
|
|
|
NM_001163817.1:c.1027C>G
|
NP_001157289.1:p.Leu343Val
|
|
NM_001360.2:c.1027C>G , LRG_340t1:c.1027C>G
|
NP_001351.2:p.Leu343Val
|
|
XM_011544777.1:c.1161C>G
|
XP_011543079.1:p.Cys387Trp
|
|
XM_011544777.2:c.1161C>G
|
XP_011543079.1:p.Cys387Trp
|
|
NM_001163817.2:c.1027C>G
|
NP_001157289.1:p.Leu343Val
|
|
NM_001360.3:c.1027C>G
MANE Select
|
NP_001351.2:p.Leu343Val
|
|