|
NM_001378454.1:c.805C>T
MANE Select
|
NP_001365383.1:p.Arg269Ter
|
|
ENST00000613296.6:c.805C>T
MANE Select
|
ENSP00000482968.1:p.Arg269Ter
|
|
NM_015120.4:c.808C>T , LRG_741t1:c.808C>T
|
NP_055935.4:p.Arg270Ter
|
|
ENST00000484298.5:c.679C>T
|
ENSP00000478155.1:p.Arg227Ter
|
|
ENST00000613296.4:c.805C>T
|
ENSP00000482968.1:p.Arg269Ter
|
|
ENST00000614410.4:c.805C>T
|
ENSP00000479094.1:p.Arg269Ter
|
|
ENST00000682565.1:c.355C>T
|
ENSP00000507671.1:p.Arg119Ter
|
|
ENST00000682675.1:n.765C>T
|
|
|
ENST00000682801.1:c.355C>T
|
ENSP00000507862.1:p.Arg119Ter
|
|
ENST00000682859.1:c.355C>T
|
ENSP00000508222.1:p.Arg119Ter
|
|
ENST00000682889.1:n.770C>T
|
|
|
ENST00000683791.1:c.159C>T
|
|
|
ENST00000684548.1:c.355C>T
|
ENSP00000507421.1:p.Arg119Ter
|