ENST00000369538.4:c.1322G>A
|
ENSP00000358551.4:p.Cys441Tyr
|
|
ENST00000520113.7:c.1334G>A
MANE Select
|
ENSP00000430075.3:p.Cys445Tyr
|
|
ENST00000637080.1:c.1117G>A
|
ENSP00000489753.1:n.1117G>A
|
|
ENST00000639077.1:n.999G>A
|
|
|
ENST00000369538.3:c.1421G>A
|
ENSP00000358551.3:p.Cys474Tyr
|
|
ENST00000520113.6:c.1433G>A
|
ENSP00000430075.2:p.Cys478Tyr
|
|
NM_000036.2:c.1433G>A
|
NP_000027.2:p.Cys478Tyr
|
|
NM_001172626.1:c.1421G>A
|
NP_001166097.1:p.Cys474Tyr
|
|
NM_000036.3:c.1334G>A
MANE Select
|
NP_000027.3:p.Cys445Tyr
|
|
NM_001172626.2:c.1322G>A
|
NP_001166097.2:p.Cys441Tyr
|
|