ENST00000682565.1:c.10213T=
|
ENSP00000507671.1:p.Tyr3405=
|
|
ENST00000682801.1:c.10213T=
|
ENSP00000507862.1:p.Tyr3405=
|
|
ENST00000682859.1:c.10213T=
|
ENSP00000508222.1:p.Tyr3405=
|
|
ENST00000683791.1:c.3299T=
|
|
|
ENST00000684460.1:c.7494T=
|
|
|
ENST00000684548.1:c.10213T=
|
ENSP00000507421.1:p.Tyr3405=
|
|
ENST00000684590.1:c.4660T=
|
ENSP00000507376.1:p.Tyr1554=
|
|
ENST00000684656.1:c.7539T=
|
|
|
ENST00000613296.6:c.10594T=
MANE Select
|
ENSP00000482968.1:p.Tyr3532=
|
|
ENST00000651057.1:c.748T=
|
ENSP00000498504.1:p.Tyr250=
|
|
ENST00000651434.1:c.1950T=
|
|
|
ENST00000652487.1:c.1691T=
|
|
|
ENST00000423048.5:c.4085T=
|
ENSP00000399833.1:n.4085T=
|
|
ENST00000484298.5:c.10468T=
|
ENSP00000478155.1:p.Tyr3490=
|
|
ENST00000613296.4:c.10594T=
|
ENSP00000482968.1:p.Tyr3532=
|
|
ENST00000614410.4:c.10594T=
|
ENSP00000479094.1:p.Tyr3532=
|
|
ENST00000620466.4:n.4397T=
|
|
|
NM_015120.4:c.10597T= , LRG_741t1:c.10597T=
|
NP_055935.4:p.Tyr3533=
|
|
NM_001378454.1:c.10594T=
MANE Select
|
NP_001365383.1:p.Tyr3532=
|
|