ENST00000496887.7:c.689A=
|
ENSP00000434560.2:p.Asp230=
|
|
ENST00000646564.2:c.506A=
|
ENSP00000495806.2:p.Asp169=
|
|
ENST00000155840.12:c.950A=
MANE Select
|
ENSP00000155840.2:p.Asp317=
|
|
ENST00000335475.6:c.569A=
|
ENSP00000334497.5:p.Asp190=
|
|
ENST00000646564.1:c.152A=
|
ENSP00000495806.1:p.Asp51=
|
|
ENST00000155840.9:c.950A=
|
ENSP00000155840.2:p.Asp317=
|
|
ENST00000335475.5:c.569A=
|
ENSP00000334497.5:p.Asp190=
|
|
NM_000218.2:c.950A= , LRG_287t1:c.950A=
|
NP_000209.2:p.Asp317=
|
|
NM_181798.1:c.569A= , LRG_287t2:c.569A=
|
NP_861463.1:p.Asp190=
|
|
NM_000218.3:c.950A=
MANE Select
|
NP_000209.2:p.Asp317=
|
|