ENST00000261304.7:c.741T>G
MANE Select
|
ENSP00000261304.2:p.Val247=
|
|
ENST00000261304.6:c.741T>G
|
ENSP00000261304.2:p.Val247=
|
|
ENST00000393568.8:c.672T>G
|
ENSP00000377198.4:p.Val224=
|
|
ENST00000393569.6:c.663T>G
|
ENSP00000377199.2:p.Val221=
|
|
ENST00000474294.6:n.731T>G
|
|
|
ENST00000477716.3:n.496T>G
|
|
|
ENST00000544807.6:c.573T>G
|
ENSP00000437513.2:p.Val191=
|
|
ENST00000554916.5:n.620T>G
|
|
|
ENST00000555000.5:c.108T>G
|
ENSP00000450472.1:p.Val36=
|
|
ENST00000557316.5:c.*139T>G
|
ENSP00000452314.1:n.*139T>G
|
|
ENST00000622264.4:c.731T>G
|
|
|
NM_000153.3:c.741T>G
|
NP_000144.2:p.Val247=
|
|
NM_001201401.1:c.672T>G
|
NP_001188330.1:p.Val224=
|
|
NM_001201402.1:c.663T>G
|
NP_001188331.1:p.Val221=
|
|
XM_011536618.1:c.573T>G
|
XP_011534920.1:p.Val191=
|
|
XM_011536618.2:c.573T>G
|
XP_011534920.1:p.Val191=
|
|
NM_000153.4:c.741T>G
MANE Select
|
NP_000144.2:p.Val247=
|
|
NM_001201401.2:c.672T>G
|
NP_001188330.1:p.Val224=
|
|
NM_001201402.2:c.663T>G
|
NP_001188331.1:p.Val221=
|
|