ENST00000682565.1:c.7604T>A
|
ENSP00000507671.1:p.Phe2535Tyr
|
|
ENST00000682801.1:c.7604T>A
|
ENSP00000507862.1:p.Phe2535Tyr
|
|
ENST00000682859.1:c.7604T>A
|
ENSP00000508222.1:p.Phe2535Tyr
|
|
ENST00000683791.1:c.996T>A
|
|
|
ENST00000684460.1:c.5056T>A
|
|
|
ENST00000684548.1:c.7604T>A
|
ENSP00000507421.1:p.Phe2535Tyr
|
|
ENST00000684590.1:c.2051T>A
|
ENSP00000507376.1:p.Phe684Tyr
|
|
ENST00000684656.1:c.5056T>A
|
|
|
ENST00000613296.6:c.7985T>A
MANE Select
|
ENSP00000482968.1:p.Phe2662Tyr
|
|
ENST00000651434.1:c.896-29831T>A
|
|
|
ENST00000423048.5:c.2816T>A
|
ENSP00000399833.1:p.Phe939Tyr
|
|
ENST00000484298.5:c.7859T>A
|
ENSP00000478155.1:p.Phe2620Tyr
|
|
ENST00000613296.4:c.7985T>A
|
ENSP00000482968.1:p.Phe2662Tyr
|
|
ENST00000614410.4:c.7985T>A
|
ENSP00000479094.1:p.Phe2662Tyr
|
|
ENST00000620466.4:n.1788T>A
|
|
|
NM_015120.4:c.7988T>A , LRG_741t1:c.7988T>A
|
NP_055935.4:p.Phe2663Tyr
|
|
NM_001378454.1:c.7985T>A
MANE Select
|
NP_001365383.1:p.Phe2662Tyr
|
|