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NM_001378454.1:c.1966G>T
MANE Select
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NP_001365383.1:p.Glu656Ter
|
|
ENST00000613296.6:c.1966G>T
MANE Select
|
ENSP00000482968.1:p.Glu656Ter
|
|
NM_015120.4:c.1969G>T , LRG_741t1:c.1969G>T
|
NP_055935.4:p.Glu657Ter
|
|
ENST00000484298.5:c.1840G>T
|
ENSP00000478155.1:p.Glu614Ter
|
|
ENST00000613296.4:c.1966G>T
|
ENSP00000482968.1:p.Glu656Ter
|
|
ENST00000614410.4:c.1966G>T
|
ENSP00000479094.1:p.Glu656Ter
|
|
ENST00000682565.1:c.1585G>T
|
ENSP00000507671.1:p.Glu529Ter
|
|
ENST00000682801.1:c.1585G>T
|
ENSP00000507862.1:p.Glu529Ter
|
|
ENST00000682859.1:c.1585G>T
|
ENSP00000508222.1:p.Glu529Ter
|
|
ENST00000683791.1:c.685+16202G>T
|
|
|
ENST00000684548.1:c.1585G>T
|
ENSP00000507421.1:p.Glu529Ter
|