ENST00000248633.9:c.2226+78G=
MANE Select
|
ENSP00000248633.4:n.2226+78G=
|
|
ENST00000248633.8:c.2226+78G=
|
ENSP00000248633.4:n.2226+78G=
|
|
ENST00000428214.5:c.2055+78G=
|
ENSP00000394413.1:n.2055+78G=
|
|
ENST00000438045.5:c.1260+78G=
|
ENSP00000410438.1:n.1260+78G=
|
|
ENST00000484913.5:n.2265+78G=
|
|
|
ENST00000496092.1:n.24+78G=
|
|
|
ENST00000496420.5:n.1902+78G=
|
|
|
NM_000466.2:c.2226+78G=
|
NP_000457.1:n.2226+78G=
|
|
NM_001282677.1:c.2055+78G=
|
NP_001269606.1:n.2055+78G=
|
|
NM_001282678.1:c.1602+78G=
|
NP_001269607.1:n.1602+78G=
|
|
XM_005250433.3:c.477+78G=
|
XP_005250490.1:n.477+78G=
|
|
XR_242246.3:n.2322+78G=
|
|
|
XM_017012319.2:c.477+78G=
|
XP_016867808.1:n.477+78G=
|
|
XR_001744808.2:n.1253+78G=
|
|
|
XR_242246.5:n.2273+78G=
|
|
|
NM_000466.3:c.2226+78G=
MANE Select
|
NP_000457.1:n.2226+78G=
|
|
NM_001282677.2:c.2055+78G=
|
NP_001269606.1:n.2055+78G=
|
|
NM_001282678.2:c.1602+78G=
|
NP_001269607.1:n.1602+78G=
|
|