ENST00000257895.10:c.369G>A
MANE Select
|
ENSP00000257895.6:p.Trp123Ter
|
|
ENST00000257895.9:c.369G>A
|
ENSP00000257895.5:p.Trp123Ter
|
|
ENST00000257899.3:c.384G>A
|
|
|
ENST00000547072.5:c.78G>A
|
ENSP00000449927.1:p.Trp26Ter
|
|
ENST00000547301.1:n.477G>A
|
|
|
ENST00000548082.1:c.369G>A
|
ENSP00000447128.1:p.Trp123Ter
|
|
ENST00000548123.1:c.300+253G>A
|
|
|
ENST00000548486.1:n.379G>A
|
|
|
ENST00000549424.1:c.*41G>A
|
ENSP00000447621.1:n.*41G>A
|
|
ENST00000550412.5:c.*41G>A
|
ENSP00000447650.1:n.*41G>A
|
|
ENST00000550608.1:n.508G>A
|
|
|
ENST00000551946.5:c.*172G>A
|
ENSP00000450201.1:n.*172G>A
|
|
ENST00000552930.5:c.78G>A
|
ENSP00000448014.1:p.Trp26Ter
|
|
ENST00000553160.1:n.406-448G>A
|
|
|
ENST00000553187.5:n.379G>A
|
|
|
NM_001199771.1:c.369G>A
|
NP_001186700.1:p.Trp123Ter
|
|
NM_002905.3:c.369G>A
|
NP_002896.2:p.Trp123Ter
|
|
NR_037658.1:n.428G>A
|
|
|
NM_001199771.2:c.369G>A
|
NP_001186700.1:p.Trp123Ter
|
|
NM_002905.5:c.369G>A
MANE Select
|
NP_002896.2:p.Trp123Ter
|
|
NM_001199771.3:c.369G>A
|
NP_001186700.1:p.Trp123Ter
|
|