ENST00000369538.4:c.1333C>T
|
ENSP00000358551.4:p.His445Tyr
|
|
ENST00000520113.7:c.1345C>T
MANE Select
|
ENSP00000430075.3:p.His449Tyr
|
|
ENST00000637080.1:c.1128C>T
|
ENSP00000489753.1:n.1128C>T
|
|
ENST00000639077.1:n.1010C>T
|
|
|
ENST00000369538.3:c.1432C>T
|
ENSP00000358551.3:p.His478Tyr
|
|
ENST00000520113.6:c.1444C>T
|
ENSP00000430075.2:p.His482Tyr
|
|
NM_000036.2:c.1444C>T
|
NP_000027.2:p.His482Tyr
|
|
NM_001172626.1:c.1432C>T
|
NP_001166097.1:p.His478Tyr
|
|
NM_000036.3:c.1345C>T
MANE Select
|
NP_000027.3:p.His449Tyr
|
|
NM_001172626.2:c.1333C>T
|
NP_001166097.2:p.His445Tyr
|
|