ENST00000295408.9:c.1460A>G
MANE Select
|
ENSP00000295408.4:p.Asp487Gly
|
|
ENST00000295408.8:c.1460A>G
|
ENSP00000295408.4:p.Asp487Gly
|
|
ENST00000409780.5:c.932A>G
|
ENSP00000387277.1:p.Asp311Gly
|
|
ENST00000421804.6:c.1460A>G
|
ENSP00000389152.2:p.Asp487Gly
|
|
ENST00000439966.5:c.*933A>G
|
ENSP00000402129.1:n.*933A>G
|
|
ENST00000616902.4:c.429A>G
|
ENSP00000482824.1:p.Arg143=
|
|
NM_006343.2:c.1460A>G
|
NP_006334.2:p.Asp487Gly
|
|
XM_005263565.3:c.1460A>G
|
XP_005263622.1:p.Asp487Gly
|
|
XM_005263568.3:c.1460A>G
|
XP_005263625.1:p.Asp487Gly
|
|
XM_011510490.1:c.1271A>G
|
XP_011508792.1:p.Asp424Gly
|
|
XM_011510491.1:c.245A>G
|
XP_011508793.1:p.Asp82Gly
|
|
XM_005263565.4:c.1460A>G
|
XP_005263622.1:p.Asp487Gly
|
|
XM_005263568.4:c.1460A>G
|
XP_005263625.1:p.Asp487Gly
|
|
XM_011510490.3:c.1271A>G
|
XP_011508792.1:p.Asp424Gly
|
|
XM_017003164.1:c.1271A>G
|
XP_016858653.1:p.Asp424Gly
|
|
XM_017003165.2:c.245A>G
|
XP_016858654.1:p.Asp82Gly
|
|
NM_006343.3:c.1460A>G
MANE Select
|
NP_006334.2:p.Asp487Gly
|
|