ENST00000369538.4:c.437A=
|
ENSP00000358551.4:p.Tyr146=
|
|
ENST00000520113.7:c.449A=
MANE Select
|
ENSP00000430075.3:p.Tyr150=
|
|
ENST00000637080.1:c.452A=
|
ENSP00000489753.1:p.Tyr151=
|
|
ENST00000639077.1:n.114A=
|
|
|
ENST00000369538.3:c.536A=
|
ENSP00000358551.3:p.Tyr179=
|
|
ENST00000485564.3:n.323A=
|
|
|
ENST00000520113.6:c.548A=
|
ENSP00000430075.2:p.Tyr183=
|
|
NM_000036.2:c.548A=
|
NP_000027.2:p.Tyr183=
|
|
NM_001172626.1:c.536A=
|
NP_001166097.1:p.Tyr179=
|
|
NM_000036.3:c.449A=
MANE Select
|
NP_000027.3:p.Tyr150=
|
|
NM_001172626.2:c.437A=
|
NP_001166097.2:p.Tyr146=
|
|