ENST00000248633.9:c.2223T>C
MANE Select
|
ENSP00000248633.4:p.Asn741=
|
|
ENST00000248633.8:c.2223T>C
|
ENSP00000248633.4:p.Asn741=
|
|
ENST00000428214.5:c.2052T>C
|
ENSP00000394413.1:p.Asn684=
|
|
ENST00000438045.5:c.1257T>C
|
ENSP00000410438.1:p.Asn419=
|
|
ENST00000484913.5:n.2262T>C
|
|
|
ENST00000496092.1:n.21T>C
|
|
|
ENST00000496420.5:n.1899T>C
|
|
|
NM_000466.2:c.2223T>C
|
NP_000457.1:p.Asn741=
|
|
NM_001282677.1:c.2052T>C
|
NP_001269606.1:p.Asn684=
|
|
NM_001282678.1:c.1599T>C
|
NP_001269607.1:p.Asn533=
|
|
XM_005250433.3:c.474T>C
|
XP_005250490.1:p.Asn158=
|
|
XR_242246.3:n.2319T>C
|
|
|
XM_017012319.2:c.474T>C
|
XP_016867808.1:p.Asn158=
|
|
XR_001744808.2:n.1250T>C
|
|
|
XR_242246.5:n.2270T>C
|
|
|
NM_000466.3:c.2223T>C
MANE Select
|
NP_000457.1:p.Asn741=
|
|
NM_001282677.2:c.2052T>C
|
NP_001269606.1:p.Asn684=
|
|
NM_001282678.2:c.1599T>C
|
NP_001269607.1:p.Asn533=
|
|