ENST00000369538.4:c.530A=
|
ENSP00000358551.4:p.Tyr177=
|
|
ENST00000520113.7:c.542A=
MANE Select
|
ENSP00000430075.3:p.Tyr181=
|
|
ENST00000637080.1:c.545A=
|
ENSP00000489753.1:p.Tyr182=
|
|
ENST00000639077.1:n.207A=
|
|
|
ENST00000369538.3:c.629A=
|
ENSP00000358551.3:p.Tyr210=
|
|
ENST00000485564.3:n.416A=
|
|
|
ENST00000520113.6:c.641A=
|
ENSP00000430075.2:p.Tyr214=
|
|
NM_000036.2:c.641A=
|
NP_000027.2:p.Tyr214=
|
|
NM_001172626.1:c.629A=
|
NP_001166097.1:p.Tyr210=
|
|
NM_000036.3:c.542A=
MANE Select
|
NP_000027.3:p.Tyr181=
|
|
NM_001172626.2:c.530A=
|
NP_001166097.2:p.Tyr177=
|
|