ENST00000248633.9:c.786G=
MANE Select
|
ENSP00000248633.4:p.Glu262=
|
|
ENST00000248633.8:c.786G=
|
ENSP00000248633.4:p.Glu262=
|
|
ENST00000428214.5:c.786G=
|
ENSP00000394413.1:p.Glu262=
|
|
ENST00000438045.5:c.274-3762G=
|
ENSP00000410438.1:n.274-3762G=
|
|
ENST00000484913.5:n.825G=
|
|
|
NM_000466.2:c.786G=
|
NP_000457.1:p.Glu262=
|
|
NM_001282677.1:c.786G=
|
NP_001269606.1:p.Glu262=
|
|
NM_001282678.1:c.162G=
|
NP_001269607.1:p.Glu54=
|
|
XR_242246.3:n.882G=
|
|
|
XR_242246.5:n.833G=
|
|
|
NM_000466.3:c.786G=
MANE Select
|
NP_000457.1:p.Glu262=
|
|
NM_001282677.2:c.786G=
|
NP_001269606.1:p.Glu262=
|
|
NM_001282678.2:c.162G=
|
NP_001269607.1:p.Glu54=
|
|