ENST00000251810.8:c.1050T>C
MANE Select
|
ENSP00000251810.3:p.Asp350=
|
|
ENST00000251810.7:c.1050T>C
|
ENSP00000251810.3:p.Asp350=
|
|
ENST00000395910.6:n.437T>C
|
|
|
ENST00000395912.6:c.894T>C
|
ENSP00000379248.2:p.Asp298=
|
|
ENST00000519317.5:c.414T>C
|
ENSP00000430641.1:p.Asp138=
|
|
ENST00000519962.5:c.195T>C
|
ENSP00000429140.1:p.Asp65=
|
|
ENST00000522368.5:c.1219T>C
|
|
|
ENST00000522394.1:c.383T>C
|
ENSP00000429578.1:n.383T>C
|
|
ENST00000621845.1:c.888T>C
|
ENSP00000484318.1:p.Asp296=
|
|
NM_001172477.1:c.1266T>C , LRG_788t1:c.1266T>C
|
NP_001165948.1:p.Asp422=
|
|
NM_001172478.1:c.894T>C
|
NP_001165949.1:p.Asp298=
|
|
NM_015713.4:c.1050T>C , LRG_788t2:c.1050T>C
|
NP_056528.2:p.Asp350=
|
|
NM_001172478.2:c.894T>C
|
NP_001165949.1:p.Asp298=
|
|
NM_015713.5:c.1050T>C
MANE Select
|
NP_056528.2:p.Asp350=
|
|