ENST00000369538.4:c.22+2003C>G
|
ENSP00000358551.4:n.22+2003C>G
|
|
ENST00000520113.7:c.23C>G
MANE Select
|
ENSP00000430075.3:p.Ala8Gly
|
|
ENST00000637080.1:c.37+1990C>G
|
ENSP00000489753.1:n.37+1990C>G
|
|
ENST00000369538.3:c.121+2003C>G
|
ENSP00000358551.3:n.121+2003C>G
|
|
ENST00000520113.6:c.122C>G
|
ENSP00000430075.2:p.Ala41Gly
|
|
NM_000036.2:c.122C>G
|
NP_000027.2:p.Ala41Gly
|
|
NM_001172626.1:c.121+2003C>G
|
NP_001166097.1:n.121+2003C>G
|
|
NM_000036.3:c.23C>G
MANE Select
|
NP_000027.3:p.Ala8Gly
|
|
NM_001172626.2:c.22+2003C>G
|
NP_001166097.2:n.22+2003C>G
|
|