ENST00000261304.7:c.539T>A
MANE Select
|
ENSP00000261304.2:p.Val180Glu
|
|
ENST00000261304.6:c.539T>A
|
ENSP00000261304.2:p.Val180Glu
|
|
ENST00000393568.8:c.470T>A
|
ENSP00000377198.4:p.Val157Glu
|
|
ENST00000393569.6:c.461T>A
|
ENSP00000377199.2:p.Val154Glu
|
|
ENST00000474294.6:n.529T>A
|
|
|
ENST00000544807.6:c.371T>A
|
ENSP00000437513.2:p.Val124Glu
|
|
ENST00000554372.5:c.*288T>A
|
ENSP00000451884.1:n.*288T>A
|
|
ENST00000554916.5:n.418T>A
|
|
|
ENST00000556261.5:n.240T>A
|
|
|
ENST00000557316.5:c.539T>A
|
ENSP00000452314.1:p.Val180Glu
|
|
ENST00000622264.4:c.529T>A
|
|
|
NM_000153.3:c.539T>A
|
NP_000144.2:p.Val180Glu
|
|
NM_001201401.1:c.470T>A
|
NP_001188330.1:p.Val157Glu
|
|
NM_001201402.1:c.461T>A
|
NP_001188331.1:p.Val154Glu
|
|
XM_011536618.1:c.371T>A
|
XP_011534920.1:p.Val124Glu
|
|
XM_011536618.2:c.371T>A
|
XP_011534920.1:p.Val124Glu
|
|
NM_000153.4:c.539T>A
MANE Select
|
NP_000144.2:p.Val180Glu
|
|
NM_001201401.2:c.470T>A
|
NP_001188330.1:p.Val157Glu
|
|
NM_001201402.2:c.461T>A
|
NP_001188331.1:p.Val154Glu
|
|