ENST00000262367.10:c.3993C>G
MANE Select
|
ENSP00000262367.5:p.Thr1331=
|
|
ENST00000262367.9:c.3993C>G
|
ENSP00000262367.5:p.Thr1331=
|
|
ENST00000382070.7:c.3879C>G
|
ENSP00000371502.3:p.Thr1293=
|
|
ENST00000570939.2:c.2628C>G
|
ENSP00000461002.2:p.Thr876=
|
|
ENST00000572569.1:n.457C>G
|
|
|
ENST00000573517.6:c.299C>G
|
|
|
ENST00000574740.1:n.75C>G
|
|
|
ENST00000576720.1:n.2930C>G
|
|
|
NM_001079846.1:c.3879C>G
|
NP_001073315.1:p.Thr1293=
|
|
NM_004380.2:c.3993C>G
|
NP_004371.2:p.Thr1331=
|
|
XM_005255124.3:c.3948C>G
|
XP_005255181.1:p.Thr1316=
|
|
XM_005255125.3:c.3576C>G
|
XP_005255182.1:p.Thr1192=
|
|
XM_006720848.2:c.3993C>G
|
XP_006720911.1:p.Thr1331=
|
|
XM_011522380.1:c.3939C>G
|
XP_011520682.1:p.Thr1313=
|
|
XM_011522381.1:c.3240C>G
|
XP_011520683.1:p.Thr1080=
|
|
XM_005255124.4:c.3948C>G
|
XP_005255181.1:p.Thr1316=
|
|
XM_005255125.4:c.3576C>G
|
XP_005255182.1:p.Thr1192=
|
|
XM_006720848.3:c.3993C>G
|
XP_006720911.1:p.Thr1331=
|
|
XM_011522381.2:c.3240C>G
|
XP_011520683.1:p.Thr1080=
|
|
XM_017022944.1:c.3987C>G
|
XP_016878433.1:p.Thr1329=
|
|
NM_004380.3:c.3993C>G
MANE Select
|
NP_004371.2:p.Thr1331=
|
|