ENST00000682565.1:c.7670T>A
|
ENSP00000507671.1:p.Val2557Glu
|
|
ENST00000682801.1:c.7670T>A
|
ENSP00000507862.1:p.Val2557Glu
|
|
ENST00000682859.1:c.7670T>A
|
ENSP00000508222.1:p.Val2557Glu
|
|
ENST00000683791.1:c.1062T>A
|
|
|
ENST00000684460.1:c.5122T>A
|
|
|
ENST00000684548.1:c.7670T>A
|
ENSP00000507421.1:p.Val2557Glu
|
|
ENST00000684590.1:c.2117T>A
|
ENSP00000507376.1:p.Val706Glu
|
|
ENST00000684656.1:c.5122T>A
|
|
|
ENST00000613296.6:c.8051T>A
MANE Select
|
ENSP00000482968.1:p.Val2684Glu
|
|
ENST00000651434.1:c.896-29765T>A
|
|
|
ENST00000423048.5:c.2882T>A
|
ENSP00000399833.1:p.Val961Glu
|
|
ENST00000484298.5:c.7925T>A
|
ENSP00000478155.1:p.Val2642Glu
|
|
ENST00000613296.4:c.8051T>A
|
ENSP00000482968.1:p.Val2684Glu
|
|
ENST00000614410.4:c.8051T>A
|
ENSP00000479094.1:p.Val2684Glu
|
|
ENST00000620466.4:n.1854T>A
|
|
|
NM_015120.4:c.8054T>A , LRG_741t1:c.8054T>A
|
NP_055935.4:p.Val2685Glu
|
|
NM_001378454.1:c.8051T>A
MANE Select
|
NP_001365383.1:p.Val2684Glu
|
|