ENST00000682565.1:c.10110C>A
|
ENSP00000507671.1:p.Cys3370Ter
|
|
ENST00000682801.1:c.10110C>A
|
ENSP00000507862.1:p.Cys3370Ter
|
|
ENST00000682859.1:c.10110C>A
|
ENSP00000508222.1:p.Cys3370Ter
|
|
ENST00000683791.1:c.3196C>A
|
|
|
ENST00000684460.1:c.7391C>A
|
|
|
ENST00000684548.1:c.10110C>A
|
ENSP00000507421.1:p.Cys3370Ter
|
|
ENST00000684590.1:c.4557C>A
|
ENSP00000507376.1:p.Cys1519Ter
|
|
ENST00000684656.1:c.7436C>A
|
|
|
ENST00000613296.6:c.10491C>A
MANE Select
|
ENSP00000482968.1:p.Cys3497Ter
|
|
ENST00000651057.1:c.645C>A
|
ENSP00000498504.1:p.Cys215Ter
|
|
ENST00000651434.1:c.1847C>A
|
|
|
ENST00000652487.1:c.1588C>A
|
|
|
ENST00000423048.5:c.3982C>A
|
ENSP00000399833.1:n.3982C>A
|
|
ENST00000484298.5:c.10365C>A
|
ENSP00000478155.1:p.Cys3455Ter
|
|
ENST00000613296.4:c.10491C>A
|
ENSP00000482968.1:p.Cys3497Ter
|
|
ENST00000614410.4:c.10491C>A
|
ENSP00000479094.1:p.Cys3497Ter
|
|
ENST00000620466.4:n.4294C>A
|
|
|
NM_015120.4:c.10494C>A , LRG_741t1:c.10494C>A
|
NP_055935.4:p.Cys3498Ter
|
|
NM_001378454.1:c.10491C>A
MANE Select
|
NP_001365383.1:p.Cys3497Ter
|
|