|
NM_001378454.1:c.1266C>G
MANE Select
|
NP_001365383.1:p.Asp422Glu
|
|
ENST00000613296.6:c.1266C>G
MANE Select
|
ENSP00000482968.1:p.Asp422Glu
|
|
NM_015120.4:c.1269C>G , LRG_741t1:c.1269C>G
|
NP_055935.4:p.Asp423Glu
|
|
ENST00000484298.5:c.1140C>G
|
ENSP00000478155.1:p.Asp380Glu
|
|
ENST00000613296.4:c.1266C>G
|
ENSP00000482968.1:p.Asp422Glu
|
|
ENST00000614410.4:c.1266C>G
|
ENSP00000479094.1:p.Asp422Glu
|
|
ENST00000682565.1:c.816C>G
|
ENSP00000507671.1:p.Asp272Glu
|
|
ENST00000682801.1:c.816C>G
|
ENSP00000507862.1:p.Asp272Glu
|
|
ENST00000682859.1:c.816C>G
|
ENSP00000508222.1:p.Asp272Glu
|
|
ENST00000682889.1:n.1231C>G
|
|
|
ENST00000683791.1:c.591+1579C>G
|
|
|
ENST00000684548.1:c.816C>G
|
ENSP00000507421.1:p.Asp272Glu
|