ENST00000251810.8:c.1055A>G
MANE Select
|
ENSP00000251810.3:p.Ter352=
|
|
ENST00000251810.7:c.1055A>G
|
ENSP00000251810.3:p.Ter352=
|
|
ENST00000395910.6:n.442A>G
|
|
|
ENST00000395912.6:c.899A>G
|
ENSP00000379248.2:p.Ter300=
|
|
ENST00000519317.5:c.419A>G
|
ENSP00000430641.1:p.Ter140=
|
|
ENST00000519962.5:c.200A>G
|
ENSP00000429140.1:p.Ter67=
|
|
ENST00000522368.5:c.1224A>G
|
|
|
ENST00000522394.1:c.388A>G
|
ENSP00000429578.1:n.388A>G
|
|
ENST00000621845.1:c.893A>G
|
ENSP00000484318.1:p.Ter298=
|
|
NM_001172477.1:c.1271A>G , LRG_788t1:c.1271A>G
|
NP_001165948.1:p.Ter424=
|
|
NM_001172478.1:c.899A>G
|
NP_001165949.1:p.Ter300=
|
|
NM_015713.4:c.1055A>G , LRG_788t2:c.1055A>G
|
NP_056528.2:p.Ter352=
|
|
NM_001172478.2:c.899A>G
|
NP_001165949.1:p.Ter300=
|
|
NM_015713.5:c.1055A>G
MANE Select
|
NP_056528.2:p.Ter352=
|
|