ENST00000379644.9:c.974G>T
MANE Select
|
ENSP00000368965.4:p.Gly325Val
|
|
ENST00000379644.8:c.974G>T
|
ENSP00000368965.4:p.Gly325Val
|
|
ENST00000522082.5:c.215G>T
|
ENSP00000430151.1:p.Gly72Val
|
|
ENST00000524016.5:c.78G>T
|
|
|
NM_152419.2:c.974G>T
|
NP_689632.2:p.Gly325Val
|
|
XM_005273409.1:c.974G>T
|
XP_005273466.1:p.Gly325Val
|
|
XM_005273410.1:c.974G>T
|
XP_005273467.1:p.Gly325Val
|
|
XM_005273411.1:c.821-3949G>T
|
XP_005273468.1:n.821-3949G>T
|
|
XM_005273412.2:c.974G>T
|
XP_005273469.1:p.Gly325Val
|
|
NM_001363227.1:c.974G>T
|
NP_001350156.1:p.Gly325Val
|
|
NM_001363228.1:c.821-3949G>T
|
NP_001350157.1:n.821-3949G>T
|
|
NM_001363229.1:c.110G>T
|
NP_001350158.1:p.Gly37Val
|
|
XM_005273412.4:c.974G>T
|
XP_005273469.1:p.Gly325Val
|
|
NM_152419.3:c.974G>T
MANE Select
|
NP_689632.2:p.Gly325Val
|
|
NM_001363227.2:c.974G>T
|
NP_001350156.1:p.Gly325Val
|
|
NM_001363228.2:c.821-3949G>T
|
NP_001350157.1:n.821-3949G>T
|
|
NM_001363229.2:c.110G>T
|
NP_001350158.1:p.Gly37Val
|
|