ENST00000414306.6:c.*380T=
|
ENSP00000394586.1:n.*380T=
|
|
ENST00000697860.1:n.616T=
|
|
|
ENST00000697861.1:c.448T=
|
ENSP00000513460.1:p.Phe150=
|
|
ENST00000697862.1:c.*90T=
|
ENSP00000513461.1:n.*90T=
|
|
ENST00000697863.1:c.592T=
|
ENSP00000513462.1:p.Phe198=
|
|
ENST00000697864.1:n.1793T=
|
|
|
ENST00000697865.1:c.592T=
|
ENSP00000513463.1:p.Phe198=
|
|
ENST00000697866.1:c.331T=
|
ENSP00000513464.1:p.Phe111=
|
|
ENST00000697867.1:c.627T=
|
|
|
ENST00000697868.1:c.*413T=
|
ENSP00000513466.1:n.*413T=
|
|
ENST00000697897.1:c.649T=
|
ENSP00000513469.1:p.Phe217=
|
|
ENST00000246868.7:c.649T=
MANE Select
|
ENSP00000246868.2:p.Phe217=
|
|
ENST00000246868.6:c.649T=
|
ENSP00000246868.2:p.Phe217=
|
|
ENST00000414306.5:c.*380T=
|
ENSP00000394586.1:n.*380T=
|
|
ENST00000617799.1:c.649T=
|
ENSP00000483040.1:p.Phe217=
|
|
NM_016038.2:c.649T= , LRG_104t1:c.649T=
|
NP_057122.2:p.Phe217=
|
|
NM_016038.3:c.649T=
|
NP_057122.2:p.Phe217=
|
|
NM_016038.4:c.649T=
MANE Select
|
NP_057122.2:p.Phe217=
|
|