ENST00000682565.1:c.7868T>A
|
ENSP00000507671.1:p.Phe2623Tyr
|
|
ENST00000682801.1:c.7868T>A
|
ENSP00000507862.1:p.Phe2623Tyr
|
|
ENST00000682859.1:c.7868T>A
|
ENSP00000508222.1:p.Phe2623Tyr
|
|
ENST00000683791.1:c.1260T>A
|
|
|
ENST00000684460.1:c.5320T>A
|
|
|
ENST00000684548.1:c.7868T>A
|
ENSP00000507421.1:p.Phe2623Tyr
|
|
ENST00000684590.1:c.2315T>A
|
ENSP00000507376.1:p.Phe772Tyr
|
|
ENST00000684656.1:c.5320T>A
|
|
|
ENST00000613296.6:c.8249T>A
MANE Select
|
ENSP00000482968.1:p.Phe2750Tyr
|
|
ENST00000651434.1:c.896-29567T>A
|
|
|
ENST00000423048.5:c.3030+50T>A
|
ENSP00000399833.1:n.3030+50T>A
|
|
ENST00000484298.5:c.8123T>A
|
ENSP00000478155.1:p.Phe2708Tyr
|
|
ENST00000613296.4:c.8249T>A
|
ENSP00000482968.1:p.Phe2750Tyr
|
|
ENST00000614410.4:c.8249T>A
|
ENSP00000479094.1:p.Phe2750Tyr
|
|
ENST00000620466.4:n.2052T>A
|
|
|
NM_015120.4:c.8252T>A , LRG_741t1:c.8252T>A
|
NP_055935.4:p.Phe2751Tyr
|
|
NM_001378454.1:c.8249T>A
MANE Select
|
NP_001365383.1:p.Phe2750Tyr
|
|