ENST00000248633.9:c.2367T=
MANE Select
|
ENSP00000248633.4:p.Asp789=
|
|
ENST00000248633.8:c.2367T=
|
ENSP00000248633.4:p.Asp789=
|
|
ENST00000428214.5:c.2196T=
|
ENSP00000394413.1:p.Asp732=
|
|
ENST00000438045.5:c.1401T=
|
ENSP00000410438.1:p.Asp467=
|
|
ENST00000484913.5:n.2406T=
|
|
|
ENST00000496092.1:n.165T=
|
|
|
ENST00000496420.5:n.2043T=
|
|
|
NM_000466.2:c.2367T=
|
NP_000457.1:p.Asp789=
|
|
NM_001282677.1:c.2196T=
|
NP_001269606.1:p.Asp732=
|
|
NM_001282678.1:c.1743T=
|
NP_001269607.1:p.Asp581=
|
|
XM_005250433.3:c.618T=
|
XP_005250490.1:p.Asp206=
|
|
XR_242246.3:n.2463T=
|
|
|
XM_017012319.2:c.618T=
|
XP_016867808.1:p.Asp206=
|
|
XR_001744808.2:n.1394T=
|
|
|
XR_242246.5:n.2414T=
|
|
|
NM_000466.3:c.2367T=
MANE Select
|
NP_000457.1:p.Asp789=
|
|
NM_001282677.2:c.2196T=
|
NP_001269606.1:p.Asp732=
|
|
NM_001282678.2:c.1743T=
|
NP_001269607.1:p.Asp581=
|
|