ENST00000251810.8:c.1026T>G
MANE Select
|
ENSP00000251810.3:p.Asp342Glu
|
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ENST00000251810.7:c.1026T>G
|
ENSP00000251810.3:p.Asp342Glu
|
|
ENST00000395910.6:n.413T>G
|
|
|
ENST00000395912.6:c.870T>G
|
ENSP00000379248.2:p.Asp290Glu
|
|
ENST00000519317.5:c.390T>G
|
ENSP00000430641.1:p.Asp130Glu
|
|
ENST00000519962.5:c.171T>G
|
ENSP00000429140.1:p.Asp57Glu
|
|
ENST00000522368.5:c.1195T>G
|
|
|
ENST00000522394.1:c.359T>G
|
ENSP00000429578.1:n.359T>G
|
|
ENST00000621845.1:c.864T>G
|
ENSP00000484318.1:p.Asp288Glu
|
|
NM_001172477.1:c.1242T>G , LRG_788t1:c.1242T>G
|
NP_001165948.1:p.Asp414Glu
|
|
NM_001172478.1:c.870T>G
|
NP_001165949.1:p.Asp290Glu
|
|
NM_015713.4:c.1026T>G , LRG_788t2:c.1026T>G
|
NP_056528.2:p.Asp342Glu
|
|
NM_001172478.2:c.870T>G
|
NP_001165949.1:p.Asp290Glu
|
|
NM_015713.5:c.1026T>G
MANE Select
|
NP_056528.2:p.Asp342Glu
|
|