ENST00000248633.9:c.2190A>T
MANE Select
|
ENSP00000248633.4:p.Ile730=
|
|
ENST00000248633.8:c.2190A>T
|
ENSP00000248633.4:p.Ile730=
|
|
ENST00000428214.5:c.2019A>T
|
ENSP00000394413.1:p.Ile673=
|
|
ENST00000438045.5:c.1224A>T
|
ENSP00000410438.1:p.Ile408=
|
|
ENST00000484913.5:n.2229A>T
|
|
|
ENST00000496420.5:n.1866A>T
|
|
|
NM_000466.2:c.2190A>T
|
NP_000457.1:p.Ile730=
|
|
NM_001282677.1:c.2019A>T
|
NP_001269606.1:p.Ile673=
|
|
NM_001282678.1:c.1566A>T
|
NP_001269607.1:p.Ile522=
|
|
XM_005250433.3:c.441A>T
|
XP_005250490.1:p.Ile147=
|
|
XR_242246.3:n.2286A>T
|
|
|
XM_017012319.2:c.441A>T
|
XP_016867808.1:p.Ile147=
|
|
XR_001744808.2:n.1217A>T
|
|
|
XR_242246.5:n.2237A>T
|
|
|
NM_000466.3:c.2190A>T
MANE Select
|
NP_000457.1:p.Ile730=
|
|
NM_001282677.2:c.2019A>T
|
NP_001269606.1:p.Ile673=
|
|
NM_001282678.2:c.1566A>T
|
NP_001269607.1:p.Ile522=
|
|