ENST00000682565.1:c.10556T>A
|
ENSP00000507671.1:p.Val3519Asp
|
|
ENST00000682801.1:c.10556T>A
|
ENSP00000507862.1:p.Val3519Asp
|
|
ENST00000682859.1:c.10556T>A
|
ENSP00000508222.1:p.Val3519Asp
|
|
ENST00000683791.1:c.3642T>A
|
|
|
ENST00000684460.1:c.7837T>A
|
|
|
ENST00000684548.1:c.10556T>A
|
ENSP00000507421.1:p.Val3519Asp
|
|
ENST00000684590.1:c.5003T>A
|
ENSP00000507376.1:p.Val1668Asp
|
|
ENST00000684656.1:c.7882T>A
|
|
|
ENST00000613296.6:c.10937T>A
MANE Select
|
ENSP00000482968.1:p.Val3646Asp
|
|
ENST00000651057.1:c.1091T>A
|
ENSP00000498504.1:p.Val364Asp
|
|
ENST00000651434.1:c.2293T>A
|
|
|
ENST00000651750.1:c.325T>A
|
|
|
ENST00000652487.1:c.2034T>A
|
|
|
ENST00000423048.5:c.4428T>A
|
ENSP00000399833.1:n.4428T>A
|
|
ENST00000484298.5:c.10811T>A
|
ENSP00000478155.1:p.Val3604Asp
|
|
ENST00000613296.4:c.10937T>A
|
ENSP00000482968.1:p.Val3646Asp
|
|
ENST00000614410.4:c.10937T>A
|
ENSP00000479094.1:p.Val3646Asp
|
|
ENST00000620466.4:n.4740T>A
|
|
|
NM_015120.4:c.10940T>A , LRG_741t1:c.10940T>A
|
NP_055935.4:p.Val3647Asp
|
|
NM_001378454.1:c.10937T>A
MANE Select
|
NP_001365383.1:p.Val3646Asp
|
|