ENST00000356518.7:c.1688T>A
MANE Select
|
ENSP00000348912.3:p.Phe563Tyr
|
|
ENST00000350009.6:c.1688T>A
|
ENSP00000322550.5:p.Phe563Tyr
|
|
ENST00000356518.6:c.1688T>A
|
ENSP00000348912.2:p.Phe563Tyr
|
|
ENST00000379861.8:c.1688T>A
|
ENSP00000369190.4:p.Phe563Tyr
|
|
ENST00000466620.5:n.1327T>A
|
|
|
ENST00000617732.1:c.*632-438T>A
|
ENSP00000483343.1:n.*632-438T>A
|
|
ENST00000619289.4:c.1328T>A
|
ENSP00000484600.1:p.Phe443Tyr
|
|
NM_001282447.1:c.1688T>A
|
NP_001269376.1:p.Phe563Tyr
|
|
NM_025220.3:c.1688T>A
|
NP_079496.1:p.Phe563Tyr
|
|
NM_153202.2:c.1688T>A
|
NP_694882.1:p.Phe563Tyr
|
|
XM_005260843.1:c.1727T>A
|
XP_005260900.1:p.Phe576Tyr
|
|
XM_006723639.1:c.1727T>A
|
XP_006723702.1:p.Phe576Tyr
|
|
XM_006723640.1:c.1718T>A
|
XP_006723703.1:p.Phe573Tyr
|
|
XM_011529366.1:c.1724T>A
|
XP_011527668.1:p.Phe575Tyr
|
|
XM_011529367.1:c.1685T>A
|
XP_011527669.1:p.Phe562Tyr
|
|
XM_011529368.1:c.1727T>A
|
XP_011527670.1:p.Phe576Tyr
|
|
XM_011529369.1:c.1695T>A
|
XP_011527671.1:p.Leu565=
|
|
XM_011529370.1:c.1695T>A
|
XP_011527672.1:p.Leu565=
|
|
XM_011529373.1:c.725T>A
|
XP_011527675.1:p.Phe242Tyr
|
|
XR_937151.1:n.1831T>A
|
|
|
XR_937152.1:n.1831T>A
|
|
|
XR_937153.1:n.1712T>A
|
|
|
XR_937154.1:n.1712T>A
|
|
|
XR_937155.1:n.1633T>A
|
|
|
XR_937157.1:n.1635T>A
|
|
|
NM_001282447.2:c.1688T>A
|
NP_001269376.1:p.Phe563Tyr
|
|
NM_025220.4:c.1688T>A
|
NP_079496.1:p.Phe563Tyr
|
|
NM_153202.3:c.1688T>A
|
NP_694882.1:p.Phe563Tyr
|
|
XM_011529373.2:c.725T>A
|
XP_011527675.1:p.Phe242Tyr
|
|
XR_001754405.1:n.1799T>A
|
|
|
XR_002958534.1:n.1908T>A
|
|
|
NM_001282447.3:c.1688T>A
|
NP_001269376.1:p.Phe563Tyr
|
|
NM_025220.5:c.1688T>A
MANE Select
|
NP_079496.1:p.Phe563Tyr
|
|
NM_153202.4:c.1688T>A
|
NP_694882.1:p.Phe563Tyr
|
|