ENST00000379644.9:c.1041T>A
MANE Select
|
ENSP00000368965.4:p.Gly347=
|
|
ENST00000379644.8:c.1041T>A
|
ENSP00000368965.4:p.Gly347=
|
|
ENST00000519000.1:n.527T>A
|
|
|
ENST00000521576.1:c.192T>A
|
ENSP00000429029.1:p.Gly64=
|
|
ENST00000522082.5:c.282T>A
|
ENSP00000430151.1:p.Gly94=
|
|
ENST00000524016.5:c.145T>A
|
|
|
NM_152419.2:c.1041T>A
|
NP_689632.2:p.Gly347=
|
|
XM_005273409.1:c.1041T>A
|
XP_005273466.1:p.Gly347=
|
|
XM_005273410.1:c.1041T>A
|
XP_005273467.1:p.Gly347=
|
|
XM_005273411.1:c.849T>A
|
XP_005273468.1:p.Gly283=
|
|
XM_005273412.2:c.1041T>A
|
XP_005273469.1:p.Gly347=
|
|
NM_001363227.1:c.1041T>A
|
NP_001350156.1:p.Gly347=
|
|
NM_001363228.1:c.849T>A
|
NP_001350157.1:p.Gly283=
|
|
NM_001363229.1:c.177T>A
|
NP_001350158.1:p.Gly59=
|
|
XM_005273412.4:c.1041T>A
|
XP_005273469.1:p.Gly347=
|
|
NM_152419.3:c.1041T>A
MANE Select
|
NP_689632.2:p.Gly347=
|
|
NM_001363227.2:c.1041T>A
|
NP_001350156.1:p.Gly347=
|
|
NM_001363228.2:c.849T>A
|
NP_001350157.1:p.Gly283=
|
|
NM_001363229.2:c.177T>A
|
NP_001350158.1:p.Gly59=
|
|