ENST00000369538.4:c.827T>G
|
ENSP00000358551.4:p.Met276Arg
|
|
ENST00000520113.7:c.839T>G
MANE Select
|
ENSP00000430075.3:p.Met280Arg
|
|
ENST00000637080.1:c.622T>G
|
ENSP00000489753.1:n.622T>G
|
|
ENST00000639077.1:n.504T>G
|
|
|
ENST00000369538.3:c.926T>G
|
ENSP00000358551.3:p.Met309Arg
|
|
ENST00000520113.6:c.938T>G
|
ENSP00000430075.2:p.Met313Arg
|
|
NM_000036.2:c.938T>G
|
NP_000027.2:p.Met313Arg
|
|
NM_001172626.1:c.926T>G
|
NP_001166097.1:p.Met309Arg
|
|
NM_000036.3:c.839T>G
MANE Select
|
NP_000027.3:p.Met280Arg
|
|
NM_001172626.2:c.827T>G
|
NP_001166097.2:p.Met276Arg
|
|