ENST00000302804.12:c.594A>T
MANE Select
|
ENSP00000302898.6:p.Thr198=
|
|
ENST00000302804.11:c.594A>T
|
ENSP00000302898.6:p.Thr198=
|
|
ENST00000415300.6:c.537A>T
|
ENSP00000407162.1:p.Thr179=
|
|
ENST00000448930.5:c.489A>T
|
ENSP00000406798.2:p.Thr163=
|
|
ENST00000594599.1:c.78A>T
|
ENSP00000469894.1:p.Thr26=
|
|
ENST00000596375.1:c.*155A>T
|
ENSP00000470465.1:n.*155A>T
|
|
ENST00000598785.5:c.492A>T
|
ENSP00000471830.1:p.Thr164=
|
|
ENST00000599062.5:c.585A>T
|
ENSP00000469983.1:p.Thr195=
|
|
ENST00000601799.5:c.*893A>T
|
ENSP00000468918.1:n.*893A>T
|
|
NM_001015878.1:c.594A>T
|
NP_001015878.1:p.Thr198=
|
|
NM_001015879.1:c.537A>T
|
NP_001015879.1:p.Thr179=
|
|
NM_003160.2:c.492A>T
|
NP_003151.2:p.Thr164=
|
|
XR_430209.2:n.1488A>T
|
|
|
XR_430209.3:n.1531A>T
|
|
|
NM_001015878.2:c.594A>T
MANE Select
|
NP_001015878.1:p.Thr198=
|
|
NM_001015879.2:c.537A>T
|
NP_001015879.1:p.Thr179=
|
|
NM_003160.3:c.492A>T
|
NP_003151.2:p.Thr164=
|
|