ENST00000430325.7:c.152G>A
MANE Select
|
ENSP00000396755.2:p.Gly51Asp
|
|
ENST00000599263.6:c.152G>A
|
ENSP00000470643.2:p.Gly51Asp
|
|
ENST00000221818.5:c.152G>A
|
ENSP00000221818.1:p.Gly51Asp
|
|
ENST00000430325.6:c.152G>A
|
ENSP00000396755.2:p.Gly51Asp
|
|
NM_024877.3:c.152G>A
|
NP_079153.2:p.Gly51Asp
|
|
XM_006723395.2:c.356G>A
|
XP_006723458.2:p.Gly119Asp
|
|
XR_430212.2:n.606G>A
|
|
|
XR_935860.1:n.606G>A
|
|
|
XR_935861.1:n.606G>A
|
|
|
XM_006723395.3:c.356G>A
|
XP_006723458.2:p.Gly119Asp
|
|
XR_001753763.1:n.622G>A
|
|
|
XR_935861.2:n.622G>A
|
|
|
NM_024877.4:c.152G>A
MANE Select
|
NP_079153.2:p.Gly51Asp
|
|