ENST00000357720.9:c.902T>A
MANE Select
|
ENSP00000350352.4:p.Leu301His
|
|
ENST00000221504.12:c.902T>A
|
ENSP00000221504.7:p.Leu301His
|
|
ENST00000357720.8:c.902T>A
|
ENSP00000350352.4:p.Leu301His
|
|
ENST00000437766.5:c.902T>A
|
ENSP00000416149.1:p.Leu301His
|
|
ENST00000587487.5:c.260T>A
|
ENSP00000465370.1:p.Leu87His
|
|
ENST00000587633.1:c.559T>A
|
ENSP00000466716.1:n.559T>A
|
|
ENST00000588511.5:n.1087T>A
|
|
|
ENST00000592062.5:c.902T>A
|
ENSP00000466967.1:p.Leu301His
|
|
ENST00000592814.5:c.776T>A
|
ENSP00000467938.1:p.Leu259His
|
|
ENST00000593157.5:n.931T>A
|
|
|
NM_001136035.2:c.902T>A
|
NP_001129507.1:p.Leu301His
|
|
NM_001142554.1:c.902T>A
|
NP_001136026.1:p.Leu301His
|
|
NM_017722.3:c.902T>A
|
NP_060192.1:p.Leu301His
|
|
XM_005259983.1:c.902T>A
|
XP_005260040.1:p.Leu301His
|
|
XM_006722793.2:c.260T>A
|
XP_006722856.1:p.Leu87His
|
|
XM_011528124.1:c.794T>A
|
XP_011526426.1:p.Leu265His
|
|
XM_011528125.1:c.260T>A
|
XP_011526427.1:p.Leu87His
|
|
XM_011528126.1:c.119T>A
|
XP_011526428.1:p.Leu40His
|
|
NM_001136035.3:c.902T>A
|
NP_001129507.1:p.Leu301His
|
|
NM_001142554.2:c.902T>A
|
NP_001136026.1:p.Leu301His
|
|
NM_001351760.1:c.902T>A
|
NP_001338689.1:p.Leu301His
|
|
NM_001351761.1:c.794T>A
|
NP_001338690.1:p.Leu265His
|
|
NM_001351762.1:c.119T>A
|
NP_001338691.1:p.Leu40His
|
|
NM_017722.4:c.902T>A
|
NP_060192.1:p.Leu301His
|
|
XM_024451587.1:c.260T>A
|
XP_024307355.1:p.Leu87His
|
|
XM_024451588.1:c.260T>A
|
XP_024307356.1:p.Leu87His
|
|
XM_024451589.1:c.260T>A
|
XP_024307357.1:p.Leu87His
|
|
XM_024451590.1:c.260T>A
|
XP_024307358.1:p.Leu87His
|
|
XM_024451591.1:c.119T>A
|
XP_024307359.1:p.Leu40His
|
|
XM_024451592.1:c.119T>A
|
XP_024307360.1:p.Leu40His
|
|
XM_024451593.1:c.119T>A
|
XP_024307361.1:p.Leu40His
|
|
XR_002958328.1:n.1028T>A
|
|
|
XR_002958329.1:n.727T>A
|
|
|
NM_001136035.4:c.902T>A
MANE Select
|
NP_001129507.1:p.Leu301His
|
|
NM_001142554.3:c.902T>A
|
NP_001136026.1:p.Leu301His
|
|
NM_001351760.2:c.902T>A
|
NP_001338689.1:p.Leu301His
|
|
NM_001351761.2:c.794T>A
|
NP_001338690.1:p.Leu265His
|
|
NM_001351762.2:c.119T>A
|
NP_001338691.1:p.Leu40His
|
|
NM_017722.5:c.902T>A
|
NP_060192.1:p.Leu301His
|
|