ENST00000369538.4:c.440T=
|
ENSP00000358551.4:p.Met147=
|
|
ENST00000520113.7:c.452T=
MANE Select
|
ENSP00000430075.3:p.Met151=
|
|
ENST00000637080.1:c.455T=
|
ENSP00000489753.1:p.Met152=
|
|
ENST00000639077.1:n.117T=
|
|
|
ENST00000369538.3:c.539T=
|
ENSP00000358551.3:p.Met180=
|
|
ENST00000485564.3:n.326T=
|
|
|
ENST00000520113.6:c.551T=
|
ENSP00000430075.2:p.Met184=
|
|
NM_000036.2:c.551T=
|
NP_000027.2:p.Met184=
|
|
NM_001172626.1:c.539T=
|
NP_001166097.1:p.Met180=
|
|
NM_000036.3:c.452T=
MANE Select
|
NP_000027.3:p.Met151=
|
|
NM_001172626.2:c.440T=
|
NP_001166097.2:p.Met147=
|
|