ENST00000682565.1:c.10490C>A
|
ENSP00000507671.1:p.Ser3497Tyr
|
|
ENST00000682801.1:c.10490C>A
|
ENSP00000507862.1:p.Ser3497Tyr
|
|
ENST00000682859.1:c.10490C>A
|
ENSP00000508222.1:p.Ser3497Tyr
|
|
ENST00000683791.1:c.3576C>A
|
|
|
ENST00000684460.1:c.7771C>A
|
|
|
ENST00000684548.1:c.10490C>A
|
ENSP00000507421.1:p.Ser3497Tyr
|
|
ENST00000684590.1:c.4937C>A
|
ENSP00000507376.1:p.Ser1646Tyr
|
|
ENST00000684656.1:c.7816C>A
|
|
|
ENST00000613296.6:c.10871C>A
MANE Select
|
ENSP00000482968.1:p.Ser3624Tyr
|
|
ENST00000651057.1:c.1025C>A
|
ENSP00000498504.1:p.Ser342Tyr
|
|
ENST00000651434.1:c.2227C>A
|
|
|
ENST00000651750.1:c.259C>A
|
|
|
ENST00000652487.1:c.1968C>A
|
|
|
ENST00000423048.5:c.4362C>A
|
ENSP00000399833.1:n.4362C>A
|
|
ENST00000484298.5:c.10745C>A
|
ENSP00000478155.1:p.Ser3582Tyr
|
|
ENST00000613296.4:c.10871C>A
|
ENSP00000482968.1:p.Ser3624Tyr
|
|
ENST00000614410.4:c.10871C>A
|
ENSP00000479094.1:p.Ser3624Tyr
|
|
ENST00000620466.4:n.4674C>A
|
|
|
NM_015120.4:c.10874C>A , LRG_741t1:c.10874C>A
|
NP_055935.4:p.Ser3625Tyr
|
|
NM_001378454.1:c.10871C>A
MANE Select
|
NP_001365383.1:p.Ser3624Tyr
|
|