ENST00000369538.4:c.498T=
|
ENSP00000358551.4:p.Asp166=
|
|
ENST00000520113.7:c.510T=
MANE Select
|
ENSP00000430075.3:p.Asp170=
|
|
ENST00000637080.1:c.513T=
|
ENSP00000489753.1:p.Asp171=
|
|
ENST00000639077.1:n.175T=
|
|
|
ENST00000369538.3:c.597T=
|
ENSP00000358551.3:p.Asp199=
|
|
ENST00000485564.3:n.384T=
|
|
|
ENST00000520113.6:c.609T=
|
ENSP00000430075.2:p.Asp203=
|
|
NM_000036.2:c.609T=
|
NP_000027.2:p.Asp203=
|
|
NM_001172626.1:c.597T=
|
NP_001166097.1:p.Asp199=
|
|
NM_000036.3:c.510T=
MANE Select
|
NP_000027.3:p.Asp170=
|
|
NM_001172626.2:c.498T=
|
NP_001166097.2:p.Asp166=
|
|