ENST00000257895.10:c.327G>A
MANE Select
|
ENSP00000257895.6:p.Val109=
|
|
ENST00000257895.9:c.327G>A
|
ENSP00000257895.5:p.Val109=
|
|
ENST00000257899.3:c.342G>A
|
|
|
ENST00000547072.5:c.36G>A
|
ENSP00000449927.1:p.Val12=
|
|
ENST00000547301.1:n.435G>A
|
|
|
ENST00000548082.1:c.327G>A
|
ENSP00000447128.1:p.Val109=
|
|
ENST00000548123.1:c.300+211G>A
|
|
|
ENST00000548486.1:n.337G>A
|
|
|
ENST00000549424.1:c.134G>A
|
ENSP00000447621.1:p.Ter45=
|
|
ENST00000550412.5:c.368G>A
|
ENSP00000447650.1:p.Ter123=
|
|
ENST00000550608.1:n.466G>A
|
|
|
ENST00000551946.5:c.*130G>A
|
ENSP00000450201.1:n.*130G>A
|
|
ENST00000552930.5:c.36G>A
|
ENSP00000448014.1:p.Val12=
|
|
ENST00000553160.1:n.406-490G>A
|
|
|
ENST00000553187.5:n.337G>A
|
|
|
NM_001199771.1:c.327G>A
|
NP_001186700.1:p.Val109=
|
|
NM_002905.3:c.327G>A
|
NP_002896.2:p.Val109=
|
|
NR_037658.1:n.386G>A
|
|
|
NM_001199771.2:c.327G>A
|
NP_001186700.1:p.Val109=
|
|
NM_002905.5:c.327G>A
MANE Select
|
NP_002896.2:p.Val109=
|
|
NM_001199771.3:c.327G>A
|
NP_001186700.1:p.Val109=
|
|