ENST00000369538.4:c.501T>G
|
ENSP00000358551.4:p.Gly167=
|
|
ENST00000520113.7:c.513T>G
MANE Select
|
ENSP00000430075.3:p.Gly171=
|
|
ENST00000637080.1:c.516T>G
|
ENSP00000489753.1:p.Gly172=
|
|
ENST00000639077.1:n.178T>G
|
|
|
ENST00000369538.3:c.600T>G
|
ENSP00000358551.3:p.Gly200=
|
|
ENST00000485564.3:n.387T>G
|
|
|
ENST00000520113.6:c.612T>G
|
ENSP00000430075.2:p.Gly204=
|
|
NM_000036.2:c.612T>G
|
NP_000027.2:p.Gly204=
|
|
NM_001172626.1:c.600T>G
|
NP_001166097.1:p.Gly200=
|
|
NM_000036.3:c.513T>G
MANE Select
|
NP_000027.3:p.Gly171=
|
|
NM_001172626.2:c.501T>G
|
NP_001166097.2:p.Gly167=
|
|