ENST00000369538.4:c.416C>G
|
ENSP00000358551.4:p.Ala139Gly
|
|
ENST00000520113.7:c.428C>G
MANE Select
|
ENSP00000430075.3:p.Ala143Gly
|
|
ENST00000637080.1:c.431C>G
|
ENSP00000489753.1:p.Ala144Gly
|
|
ENST00000639077.1:n.93C>G
|
|
|
ENST00000369538.3:c.515C>G
|
ENSP00000358551.3:p.Ala172Gly
|
|
ENST00000485564.3:n.302C>G
|
|
|
ENST00000520113.6:c.527C>G
|
ENSP00000430075.2:p.Ala176Gly
|
|
NM_000036.2:c.527C>G
|
NP_000027.2:p.Ala176Gly
|
|
NM_001172626.1:c.515C>G
|
NP_001166097.1:p.Ala172Gly
|
|
NM_000036.3:c.428C>G
MANE Select
|
NP_000027.3:p.Ala143Gly
|
|
NM_001172626.2:c.416C>G
|
NP_001166097.2:p.Ala139Gly
|
|