ENST00000369538.4:c.1288G=
|
ENSP00000358551.4:p.Asp430=
|
|
ENST00000520113.7:c.1300G=
MANE Select
|
ENSP00000430075.3:p.Asp434=
|
|
ENST00000637080.1:c.1083G=
|
ENSP00000489753.1:n.1083G=
|
|
ENST00000639077.1:n.965G=
|
|
|
ENST00000369538.3:c.1387G=
|
ENSP00000358551.3:p.Asp463=
|
|
ENST00000520113.6:c.1399G=
|
ENSP00000430075.2:p.Asp467=
|
|
NM_000036.2:c.1399G=
|
NP_000027.2:p.Asp467=
|
|
NM_001172626.1:c.1387G=
|
NP_001166097.1:p.Asp463=
|
|
NM_000036.3:c.1300G=
MANE Select
|
NP_000027.3:p.Asp434=
|
|
NM_001172626.2:c.1288G=
|
NP_001166097.2:p.Asp430=
|
|