|
ENST00000599547.6:c.5181C=
|
ENSP00000471601.2:p.Arg1727=
|
|
|
ENST00000359596.8:c.5181C=
MANE Select
|
ENSP00000352608.2:p.Arg1727=
|
|
|
ENST00000355481.8:c.5181C=
|
ENSP00000347667.3:p.Arg1727=
|
|
|
ENST00000359596.7:c.5181C=
|
ENSP00000352608.2:p.Arg1727=
|
|
|
ENST00000360985.7:c.5178C=
|
ENSP00000354254.4:p.Arg1726=
|
|
|
NM_000540.2:c.5181C= , LRG_766t1:c.5181C=
|
NP_000531.2:p.Arg1727=
|
|
|
NM_001042723.1:c.5181C=
|
NP_001036188.1:p.Arg1727=
|
|
|
XM_006723317.1:c.5181C=
|
XP_006723380.1:p.Arg1727=
|
|
|
XM_006723319.1:c.5181C=
|
XP_006723382.1:p.Arg1727=
|
|
|
XM_011527204.1:c.5178C=
|
XP_011525506.1:p.Arg1726=
|
|
|
XM_011527205.1:c.5181C=
|
XP_011525507.1:p.Arg1727=
|
|
|
XM_006723317.2:c.5181C=
|
XP_006723380.1:p.Arg1727=
|
|
|
XM_006723319.2:c.5181C=
|
XP_006723382.1:p.Arg1727=
|
|
|
XM_011527205.2:c.5181C=
|
XP_011525507.1:p.Arg1727=
|
|
|
XR_001753735.1:n.5264C=
|
|
|
|
NM_000540.3:c.5181C=
MANE Select
|
NP_000531.2:p.Arg1727=
|
|
|
NM_001042723.2:c.5181C=
|
NP_001036188.1:p.Arg1727=
|
|
