ENST00000253122.10:c.1163C>A
MANE Select
|
ENSP00000253122.5:p.Ala388Asp
|
|
ENST00000253122.9:c.1163C>A
|
ENSP00000253122.5:p.Ala388Asp
|
|
ENST00000413787.1:c.258-278C>A
|
ENSP00000400463.1:n.258-278C>A
|
|
ENST00000430077.6:c.818C>A
|
ENSP00000403041.2:p.Ala273Asp
|
|
ENST00000442457.1:c.217C>A
|
|
|
ENST00000457723.1:c.147C>A
|
ENSP00000394742.1:p.Arg49=
|
|
ENST00000467402.1:n.262C>A
|
|
|
ENST00000485324.1:n.1196C>A
|
|
|
NM_001142805.1:c.1133C>A
|
NP_001136277.1:p.Ala378Asp
|
|
NM_001142806.1:c.818C>A
|
NP_001136278.1:p.Ala273Asp
|
|
NM_005629.3:c.1163C>A
|
NP_005620.1:p.Ala388Asp
|
|
NM_005629.4:c.1163C>A
MANE Select
|
NP_005620.1:p.Ala388Asp
|
|
NM_001142805.2:c.1133C>A
|
NP_001136277.1:p.Ala378Asp
|
|