ENST00000295408.9:c.1459G=
MANE Select
|
ENSP00000295408.4:p.Asp487=
|
|
ENST00000295408.8:c.1459G=
|
ENSP00000295408.4:p.Asp487=
|
|
ENST00000409780.5:c.931G=
|
ENSP00000387277.1:p.Asp311=
|
|
ENST00000421804.6:c.1459G=
|
ENSP00000389152.2:p.Asp487=
|
|
ENST00000439966.5:c.*932G=
|
ENSP00000402129.1:n.*932G=
|
|
ENST00000616902.4:c.428G=
|
ENSP00000482824.1:p.Arg143=
|
|
NM_006343.2:c.1459G=
|
NP_006334.2:p.Asp487=
|
|
XM_005263565.3:c.1459G=
|
XP_005263622.1:p.Asp487=
|
|
XM_005263568.3:c.1459G=
|
XP_005263625.1:p.Asp487=
|
|
XM_011510490.1:c.1270G=
|
XP_011508792.1:p.Asp424=
|
|
XM_011510491.1:c.244G=
|
XP_011508793.1:p.Asp82=
|
|
XM_005263565.4:c.1459G=
|
XP_005263622.1:p.Asp487=
|
|
XM_005263568.4:c.1459G=
|
XP_005263625.1:p.Asp487=
|
|
XM_011510490.3:c.1270G=
|
XP_011508792.1:p.Asp424=
|
|
XM_017003164.1:c.1270G=
|
XP_016858653.1:p.Asp424=
|
|
XM_017003165.2:c.244G=
|
XP_016858654.1:p.Asp82=
|
|
NM_006343.3:c.1459G=
MANE Select
|
NP_006334.2:p.Asp487=
|
|