ENST00000682565.1:c.7589T>A
|
ENSP00000507671.1:p.Phe2530Tyr
|
|
ENST00000682801.1:c.7589T>A
|
ENSP00000507862.1:p.Phe2530Tyr
|
|
ENST00000682859.1:c.7589T>A
|
ENSP00000508222.1:p.Phe2530Tyr
|
|
ENST00000683791.1:c.981T>A
|
|
|
ENST00000684460.1:c.5041T>A
|
|
|
ENST00000684548.1:c.7589T>A
|
ENSP00000507421.1:p.Phe2530Tyr
|
|
ENST00000684590.1:c.2036T>A
|
ENSP00000507376.1:p.Phe679Tyr
|
|
ENST00000684656.1:c.5041T>A
|
|
|
ENST00000613296.6:c.7970T>A
MANE Select
|
ENSP00000482968.1:p.Phe2657Tyr
|
|
ENST00000651434.1:c.896-29846T>A
|
|
|
ENST00000423048.5:c.2801T>A
|
ENSP00000399833.1:p.Phe934Tyr
|
|
ENST00000484298.5:c.7844T>A
|
ENSP00000478155.1:p.Phe2615Tyr
|
|
ENST00000613296.4:c.7970T>A
|
ENSP00000482968.1:p.Phe2657Tyr
|
|
ENST00000614410.4:c.7970T>A
|
ENSP00000479094.1:p.Phe2657Tyr
|
|
ENST00000620466.4:n.1773T>A
|
|
|
NM_015120.4:c.7973T>A , LRG_741t1:c.7973T>A
|
NP_055935.4:p.Phe2658Tyr
|
|
NM_001378454.1:c.7970T>A
MANE Select
|
NP_001365383.1:p.Phe2657Tyr
|
|