ENST00000251810.8:c.979C>G
MANE Select
|
ENSP00000251810.3:p.Arg327Gly
|
|
ENST00000251810.7:c.979C>G
|
ENSP00000251810.3:p.Arg327Gly
|
|
ENST00000395910.6:n.366C>G
|
|
|
ENST00000395912.6:c.823C>G
|
ENSP00000379248.2:p.Arg275Gly
|
|
ENST00000519317.5:c.343C>G
|
ENSP00000430641.1:p.Arg115Gly
|
|
ENST00000519962.5:c.124C>G
|
ENSP00000429140.1:p.Arg42Gly
|
|
ENST00000522368.5:c.1148C>G
|
|
|
ENST00000522394.1:c.312C>G
|
ENSP00000429578.1:n.312C>G
|
|
ENST00000621845.1:c.817C>G
|
ENSP00000484318.1:p.Arg273Gly
|
|
NM_001172477.1:c.1195C>G , LRG_788t1:c.1195C>G
|
NP_001165948.1:p.Arg399Gly
|
|
NM_001172478.1:c.823C>G
|
NP_001165949.1:p.Arg275Gly
|
|
NM_015713.4:c.979C>G , LRG_788t2:c.979C>G
|
NP_056528.2:p.Arg327Gly
|
|
NM_001172478.2:c.823C>G
|
NP_001165949.1:p.Arg275Gly
|
|
NM_015713.5:c.979C>G
MANE Select
|
NP_056528.2:p.Arg327Gly
|
|