ENST00000253122.10:c.1164C>A
MANE Select
|
ENSP00000253122.5:p.Ala388=
|
|
ENST00000253122.9:c.1164C>A
|
ENSP00000253122.5:p.Ala388=
|
|
ENST00000413787.1:c.258-277C>A
|
ENSP00000400463.1:n.258-277C>A
|
|
ENST00000430077.6:c.819C>A
|
ENSP00000403041.2:p.Ala273=
|
|
ENST00000442457.1:c.218C>A
|
|
|
ENST00000457723.1:c.148C>A
|
ENSP00000394742.1:p.Leu50Ile
|
|
ENST00000467402.1:n.263C>A
|
|
|
ENST00000485324.1:n.1197C>A
|
|
|
NM_001142805.1:c.1134C>A
|
NP_001136277.1:p.Ala378=
|
|
NM_001142806.1:c.819C>A
|
NP_001136278.1:p.Ala273=
|
|
NM_005629.3:c.1164C>A
|
NP_005620.1:p.Ala388=
|
|
NM_005629.4:c.1164C>A
MANE Select
|
NP_005620.1:p.Ala388=
|
|
NM_001142805.2:c.1134C>A
|
NP_001136277.1:p.Ala378=
|
|