ENST00000682565.1:c.11665T>A
|
ENSP00000507671.1:p.Tyr3889Asn
|
|
ENST00000682801.1:c.11167-817T>A
|
ENSP00000507862.1:n.11167-817T>A
|
|
ENST00000682859.1:c.11665T>A
|
ENSP00000508222.1:p.Tyr3889Asn
|
|
ENST00000683791.1:c.4751T>A
|
|
|
ENST00000684460.1:c.8946T>A
|
|
|
ENST00000684548.1:c.11665T>A
|
ENSP00000507421.1:p.Tyr3889Asn
|
|
ENST00000684590.1:c.6112T>A
|
ENSP00000507376.1:p.Tyr2038Asn
|
|
ENST00000684656.1:c.9130T>A
|
|
|
ENST00000613296.6:c.12046T>A
MANE Select
|
ENSP00000482968.1:p.Tyr4016Asn
|
|
ENST00000651057.1:c.2200T>A
|
ENSP00000498504.1:p.Tyr734Asn
|
|
ENST00000651434.1:c.3402T>A
|
|
|
ENST00000651750.1:c.1260+487T>A
|
|
|
ENST00000652487.1:c.3217T>A
|
|
|
ENST00000464408.3:n.221T>A
|
|
|
ENST00000484298.5:c.11920T>A
|
ENSP00000478155.1:p.Tyr3974Asn
|
|
ENST00000613296.4:c.12046T>A
|
ENSP00000482968.1:p.Tyr4016Asn
|
|
ENST00000620466.4:n.5849T>A
|
|
|
NM_015120.4:c.12049T>A , LRG_741t1:c.12049T>A
|
NP_055935.4:p.Tyr4017Asn
|
|
NM_001378454.1:c.12046T>A
MANE Select
|
NP_001365383.1:p.Tyr4016Asn
|
|