ENST00000251810.8:c.1032C>G
MANE Select
|
ENSP00000251810.3:p.Val344=
|
|
ENST00000251810.7:c.1032C>G
|
ENSP00000251810.3:p.Val344=
|
|
ENST00000395910.6:n.419C>G
|
|
|
ENST00000395912.6:c.876C>G
|
ENSP00000379248.2:p.Val292=
|
|
ENST00000519317.5:c.396C>G
|
ENSP00000430641.1:p.Val132=
|
|
ENST00000519962.5:c.177C>G
|
ENSP00000429140.1:p.Val59=
|
|
ENST00000522368.5:c.1201C>G
|
|
|
ENST00000522394.1:c.365C>G
|
ENSP00000429578.1:n.365C>G
|
|
ENST00000621845.1:c.870C>G
|
ENSP00000484318.1:p.Val290=
|
|
NM_001172477.1:c.1248C>G , LRG_788t1:c.1248C>G
|
NP_001165948.1:p.Val416=
|
|
NM_001172478.1:c.876C>G
|
NP_001165949.1:p.Val292=
|
|
NM_015713.4:c.1032C>G , LRG_788t2:c.1032C>G
|
NP_056528.2:p.Val344=
|
|
NM_001172478.2:c.876C>G
|
NP_001165949.1:p.Val292=
|
|
NM_015713.5:c.1032C>G
MANE Select
|
NP_056528.2:p.Val344=
|
|