ENST00000369538.4:c.477C>G
|
ENSP00000358551.4:p.Ser159=
|
|
ENST00000520113.7:c.489C>G
MANE Select
|
ENSP00000430075.3:p.Ser163=
|
|
ENST00000637080.1:c.492C>G
|
ENSP00000489753.1:p.Ser164=
|
|
ENST00000639077.1:n.154C>G
|
|
|
ENST00000369538.3:c.576C>G
|
ENSP00000358551.3:p.Ser192=
|
|
ENST00000485564.3:n.363C>G
|
|
|
ENST00000520113.6:c.588C>G
|
ENSP00000430075.2:p.Ser196=
|
|
NM_000036.2:c.588C>G
|
NP_000027.2:p.Ser196=
|
|
NM_001172626.1:c.576C>G
|
NP_001166097.1:p.Ser192=
|
|
NM_000036.3:c.489C>G
MANE Select
|
NP_000027.3:p.Ser163=
|
|
NM_001172626.2:c.477C>G
|
NP_001166097.2:p.Ser159=
|
|