ENST00000682565.1:c.10285A>T
|
ENSP00000507671.1:p.Asn3429Tyr
|
|
ENST00000682801.1:c.10285A>T
|
ENSP00000507862.1:p.Asn3429Tyr
|
|
ENST00000682859.1:c.10285A>T
|
ENSP00000508222.1:p.Asn3429Tyr
|
|
ENST00000683791.1:c.3371A>T
|
|
|
ENST00000684460.1:c.7566A>T
|
|
|
ENST00000684548.1:c.10285A>T
|
ENSP00000507421.1:p.Asn3429Tyr
|
|
ENST00000684590.1:c.4732A>T
|
ENSP00000507376.1:p.Asn1578Tyr
|
|
ENST00000684656.1:c.7611A>T
|
|
|
ENST00000613296.6:c.10666A>T
MANE Select
|
ENSP00000482968.1:p.Asn3556Tyr
|
|
ENST00000651057.1:c.820A>T
|
ENSP00000498504.1:p.Asn274Tyr
|
|
ENST00000651434.1:c.2022A>T
|
|
|
ENST00000651750.1:c.54A>T
|
|
|
ENST00000652487.1:c.1763A>T
|
|
|
ENST00000423048.5:c.4157A>T
|
ENSP00000399833.1:n.4157A>T
|
|
ENST00000484298.5:c.10540A>T
|
ENSP00000478155.1:p.Asn3514Tyr
|
|
ENST00000613296.4:c.10666A>T
|
ENSP00000482968.1:p.Asn3556Tyr
|
|
ENST00000614410.4:c.10666A>T
|
ENSP00000479094.1:p.Asn3556Tyr
|
|
ENST00000620466.4:n.4469A>T
|
|
|
NM_015120.4:c.10669A>T , LRG_741t1:c.10669A>T
|
NP_055935.4:p.Asn3557Tyr
|
|
NM_001378454.1:c.10666A>T
MANE Select
|
NP_001365383.1:p.Asn3556Tyr
|
|