ENST00000251810.8:c.1027A>G
MANE Select
|
ENSP00000251810.3:p.Asn343Asp
|
|
ENST00000251810.7:c.1027A>G
|
ENSP00000251810.3:p.Asn343Asp
|
|
ENST00000395910.6:n.414A>G
|
|
|
ENST00000395912.6:c.871A>G
|
ENSP00000379248.2:p.Asn291Asp
|
|
ENST00000519317.5:c.391A>G
|
ENSP00000430641.1:p.Asn131Asp
|
|
ENST00000519962.5:c.172A>G
|
ENSP00000429140.1:p.Asn58Asp
|
|
ENST00000522368.5:c.1196A>G
|
|
|
ENST00000522394.1:c.360A>G
|
ENSP00000429578.1:n.360A>G
|
|
ENST00000621845.1:c.865A>G
|
ENSP00000484318.1:p.Asn289Asp
|
|
NM_001172477.1:c.1243A>G , LRG_788t1:c.1243A>G
|
NP_001165948.1:p.Asn415Asp
|
|
NM_001172478.1:c.871A>G
|
NP_001165949.1:p.Asn291Asp
|
|
NM_015713.4:c.1027A>G , LRG_788t2:c.1027A>G
|
NP_056528.2:p.Asn343Asp
|
|
NM_001172478.2:c.871A>G
|
NP_001165949.1:p.Asn291Asp
|
|
NM_015713.5:c.1027A>G
MANE Select
|
NP_056528.2:p.Asn343Asp
|
|