ENST00000369538.4:c.410A>G
|
ENSP00000358551.4:p.Tyr137Cys
|
|
ENST00000520113.7:c.422A>G
MANE Select
|
ENSP00000430075.3:p.Tyr141Cys
|
|
ENST00000637080.1:c.425A>G
|
ENSP00000489753.1:p.Tyr142Cys
|
|
ENST00000639077.1:n.87A>G
|
|
|
ENST00000369538.3:c.509A>G
|
ENSP00000358551.3:p.Tyr170Cys
|
|
ENST00000485564.3:n.296A>G
|
|
|
ENST00000520113.6:c.521A>G
|
ENSP00000430075.2:p.Tyr174Cys
|
|
NM_000036.2:c.521A>G
|
NP_000027.2:p.Tyr174Cys
|
|
NM_001172626.1:c.509A>G
|
NP_001166097.1:p.Tyr170Cys
|
|
NM_000036.3:c.422A>G
MANE Select
|
NP_000027.3:p.Tyr141Cys
|
|
NM_001172626.2:c.410A>G
|
NP_001166097.2:p.Tyr137Cys
|
|