ENST00000292180.8:c.627C>T
MANE Select
|
ENSP00000292180.3:p.Thr209=
|
|
ENST00000292180.7:c.627C>T
|
ENSP00000292180.3:p.Thr209=
|
|
ENST00000295530.6:c.-175C>T
|
ENSP00000295530.2:n.-175C>T
|
|
ENST00000315144.14:c.336C>T
|
ENSP00000317296.10:p.Thr112=
|
|
ENST00000368431.7:c.330C>T
|
ENSP00000357416.3:p.Thr110=
|
|
ENST00000368432.5:c.336C>T
|
ENSP00000357417.1:p.Thr112=
|
|
ENST00000368433.5:c.627C>T
|
ENSP00000357418.1:p.Thr209=
|
|
ENST00000487371.1:n.683C>T
|
|
|
NM_001184891.1:c.336C>T
|
NP_001171820.1:p.Thr112=
|
|
NM_001184892.1:c.330C>T
|
NP_001171821.1:p.Thr110=
|
|
NM_025207.4:c.627C>T
|
NP_079483.3:p.Thr209=
|
|
NM_201398.2:c.336C>T
|
NP_958800.1:p.Thr112=
|
|
XM_005245502.2:c.336C>T
|
XP_005245559.1:p.Thr112=
|
|
XM_005245503.2:c.-175C>T
|
XP_005245560.1:n.-175C>T
|
|
XM_006711559.2:c.336C>T
|
XP_006711622.1:p.Thr112=
|
|
XR_241098.3:n.545C>T
|
|
|
NM_025207.5:c.627C>T
MANE Select
|
NP_079483.3:p.Thr209=
|
|
NM_001184891.2:c.336C>T
|
NP_001171820.1:p.Thr112=
|
|
NM_001184892.2:c.330C>T
|
NP_001171821.1:p.Thr110=
|
|
NM_201398.3:c.336C>T
|
NP_958800.1:p.Thr112=
|
|