ENST00000682565.1:c.11518A>T
|
ENSP00000507671.1:p.Asn3840Tyr
|
|
ENST00000682801.1:c.11167-964A>T
|
ENSP00000507862.1:n.11167-964A>T
|
|
ENST00000682859.1:c.11518A>T
|
ENSP00000508222.1:p.Asn3840Tyr
|
|
ENST00000683791.1:c.4604A>T
|
|
|
ENST00000684460.1:c.8799A>T
|
|
|
ENST00000684548.1:c.11518A>T
|
ENSP00000507421.1:p.Asn3840Tyr
|
|
ENST00000684590.1:c.5965A>T
|
ENSP00000507376.1:p.Asn1989Tyr
|
|
ENST00000684656.1:c.8983A>T
|
|
|
ENST00000613296.6:c.11899A>T
MANE Select
|
ENSP00000482968.1:p.Asn3967Tyr
|
|
ENST00000651057.1:c.2053A>T
|
ENSP00000498504.1:p.Asn685Tyr
|
|
ENST00000651434.1:c.3255A>T
|
|
|
ENST00000651750.1:c.1260+340A>T
|
|
|
ENST00000652487.1:c.3070A>T
|
|
|
ENST00000464408.3:n.74A>T
|
|
|
ENST00000484298.5:c.11773A>T
|
ENSP00000478155.1:p.Asn3925Tyr
|
|
ENST00000613296.4:c.11899A>T
|
ENSP00000482968.1:p.Asn3967Tyr
|
|
ENST00000620466.4:n.5702A>T
|
|
|
NM_015120.4:c.11902A>T , LRG_741t1:c.11902A>T
|
NP_055935.4:p.Asn3968Tyr
|
|
NM_001378454.1:c.11899A>T
MANE Select
|
NP_001365383.1:p.Asn3967Tyr
|
|