ENST00000369538.4:c.918G=
|
ENSP00000358551.4:p.Met306=
|
|
ENST00000520113.7:c.930G=
MANE Select
|
ENSP00000430075.3:p.Met310=
|
|
ENST00000637080.1:c.713G=
|
ENSP00000489753.1:n.713G=
|
|
ENST00000639077.1:n.595G=
|
|
|
ENST00000369538.3:c.1017G=
|
ENSP00000358551.3:p.Met339=
|
|
ENST00000520113.6:c.1029G=
|
ENSP00000430075.2:p.Met343=
|
|
NM_000036.2:c.1029G=
|
NP_000027.2:p.Met343=
|
|
NM_001172626.1:c.1017G=
|
NP_001166097.1:p.Met339=
|
|
NM_000036.3:c.930G=
MANE Select
|
NP_000027.3:p.Met310=
|
|
NM_001172626.2:c.918G=
|
NP_001166097.2:p.Met306=
|
|