ENST00000360215.3:c.641A>T
MANE Select
|
ENSP00000353346.1:p.Asp214Val
|
|
ENST00000496656.2:n.420A>T
|
|
|
ENST00000651132.1:c.641A>T
|
ENSP00000498322.1:p.Asp214Val
|
|
ENST00000651676.1:c.641A>T
|
ENSP00000498699.1:p.Asp214Val
|
|
ENST00000651994.1:c.*70-4663A>T
|
ENSP00000498310.1:n.*70-4663A>T
|
|
ENST00000652718.1:c.473A>T
|
ENSP00000498866.1:p.Asp158Val
|
|
ENST00000360215.2:c.641A>T
|
ENSP00000353346.1:p.Asp214Val
|
|
ENST00000496656.1:n.420A>T
|
|
|
NM_182548.3:c.641A>T
|
NP_872354.1:p.Asp214Val
|
|
XM_011514403.1:c.641A>T
|
XP_011512705.1:p.Asp214Val
|
|
NM_182548.4:c.641A>T
MANE Select
|
NP_872354.1:p.Asp214Val
|
|