ENST00000369538.4:c.397T>G
|
ENSP00000358551.4:p.Cys133Gly
|
|
ENST00000520113.7:c.409T>G
MANE Select
|
ENSP00000430075.3:p.Cys137Gly
|
|
ENST00000637080.1:c.412T>G
|
ENSP00000489753.1:p.Cys138Gly
|
|
ENST00000639077.1:n.74T>G
|
|
|
ENST00000369538.3:c.496T>G
|
ENSP00000358551.3:p.Cys166Gly
|
|
ENST00000485564.3:n.283T>G
|
|
|
ENST00000520113.6:c.508T>G
|
ENSP00000430075.2:p.Cys170Gly
|
|
NM_000036.2:c.508T>G
|
NP_000027.2:p.Cys170Gly
|
|
NM_001172626.1:c.496T>G
|
NP_001166097.1:p.Cys166Gly
|
|
NM_000036.3:c.409T>G
MANE Select
|
NP_000027.3:p.Cys137Gly
|
|
NM_001172626.2:c.397T>G
|
NP_001166097.2:p.Cys133Gly
|
|