ENST00000302850.10:c.3948G>T
MANE Select
|
ENSP00000303830.4:p.Glu1316Asp
|
|
ENST00000302850.9:c.3948G>T
|
ENSP00000303830.4:p.Glu1316Asp
|
|
ENST00000341500.9:c.3912G>T
|
ENSP00000342838.4:p.Glu1304Asp
|
|
NM_000208.2:c.3948G>T
|
NP_000199.2:p.Glu1316Asp
|
|
NM_000208.3:c.3948G>T
|
NP_000199.2:p.Glu1316Asp
|
|
NM_001079817.1:c.3912G>T
|
NP_001073285.1:p.Glu1304Asp
|
|
NM_001079817.2:c.3912G>T
|
NP_001073285.1:p.Glu1304Asp
|
|
XM_011527988.1:c.4023G>T
|
XP_011526290.1:p.Glu1341Asp
|
|
XM_011527989.1:c.3987G>T
|
XP_011526291.1:p.Glu1329Asp
|
|
XM_011527988.2:c.3945G>T
|
XP_011526290.2:p.Glu1315Asp
|
|
XM_011527989.3:c.3909G>T
|
XP_011526291.2:p.Glu1303Asp
|
|
NM_000208.4:c.3948G>T
MANE Select
|
NP_000199.2:p.Glu1316Asp
|
|
NM_001079817.3:c.3912G>T
|
NP_001073285.1:p.Glu1304Asp
|
|