ENST00000414306.6:c.*88T>A
|
ENSP00000394586.1:n.*88T>A
|
|
ENST00000697860.1:n.324T>A
|
|
|
ENST00000697861.1:c.258+893T>A
|
ENSP00000513460.1:n.258+893T>A
|
|
ENST00000697862.1:c.357T>A
|
ENSP00000513461.1:p.Cys119Ter
|
|
ENST00000697863.1:c.300T>A
|
ENSP00000513462.1:p.Cys100Ter
|
|
ENST00000697864.1:n.1501T>A
|
|
|
ENST00000697865.1:c.300T>A
|
ENSP00000513463.1:p.Cys100Ter
|
|
ENST00000697866.1:c.39T>A
|
ENSP00000513464.1:p.Cys13Ter
|
|
ENST00000697867.1:c.197T>A
|
|
|
ENST00000697868.1:c.*121T>A
|
ENSP00000513466.1:n.*121T>A
|
|
ENST00000697869.1:c.*92T>A
|
ENSP00000513467.1:n.*92T>A
|
|
ENST00000697897.1:c.357T>A
|
ENSP00000513469.1:p.Cys119Ter
|
|
ENST00000246868.7:c.357T>A
MANE Select
|
ENSP00000246868.2:p.Cys119Ter
|
|
ENST00000246868.6:c.357T>A
|
ENSP00000246868.2:p.Cys119Ter
|
|
ENST00000414306.5:c.*88T>A
|
ENSP00000394586.1:n.*88T>A
|
|
ENST00000463579.1:n.246T>A
|
|
|
ENST00000490953.5:n.498T>A
|
|
|
ENST00000617799.1:c.357T>A
|
ENSP00000483040.1:p.Cys119Ter
|
|
NM_016038.2:c.357T>A , LRG_104t1:c.357T>A
|
NP_057122.2:p.Cys119Ter
|
|
NM_016038.3:c.357T>A
|
NP_057122.2:p.Cys119Ter
|
|
NM_016038.4:c.357T>A
MANE Select
|
NP_057122.2:p.Cys119Ter
|
|