ENST00000379644.9:c.1460T>A
MANE Select
|
ENSP00000368965.4:p.Val487Asp
|
|
ENST00000379644.8:c.1460T>A
|
ENSP00000368965.4:p.Val487Asp
|
|
ENST00000520678.1:n.393T>A
|
|
|
ENST00000521576.1:c.611T>A
|
ENSP00000429029.1:p.Val204Asp
|
|
ENST00000524016.5:c.564T>A
|
|
|
NM_152419.2:c.1460T>A
|
NP_689632.2:p.Val487Asp
|
|
XM_005273409.1:c.1460T>A
|
XP_005273466.1:p.Val487Asp
|
|
XM_005273410.1:c.1460T>A
|
XP_005273467.1:p.Val487Asp
|
|
XM_005273411.1:c.1268T>A
|
XP_005273468.1:p.Val423Asp
|
|
XM_005273412.2:c.1460T>A
|
XP_005273469.1:p.Val487Asp
|
|
NM_001363227.1:c.1460T>A
|
NP_001350156.1:p.Val487Asp
|
|
NM_001363228.1:c.1268T>A
|
NP_001350157.1:p.Val423Asp
|
|
NM_001363229.1:c.596T>A
|
NP_001350158.1:p.Val199Asp
|
|
XM_005273412.4:c.1460T>A
|
XP_005273469.1:p.Val487Asp
|
|
NM_152419.3:c.1460T>A
MANE Select
|
NP_689632.2:p.Val487Asp
|
|
NM_001363227.2:c.1460T>A
|
NP_001350156.1:p.Val487Asp
|
|
NM_001363228.2:c.1268T>A
|
NP_001350157.1:p.Val423Asp
|
|
NM_001363229.2:c.596T>A
|
NP_001350158.1:p.Val199Asp
|
|