ENST00000264414.9:c.1258A>G
MANE Select
|
ENSP00000264414.4:p.Arg420Gly
|
|
ENST00000264414.8:c.1258A>G
|
ENSP00000264414.4:p.Arg420Gly
|
|
ENST00000344951.8:c.1060A>G
|
ENSP00000343601.4:p.Arg354Gly
|
|
ENST00000409096.5:c.1186A>G
|
ENSP00000387200.1:p.Arg396Gly
|
|
ENST00000409777.5:c.1186A>G
|
ENSP00000386525.1:p.Arg396Gly
|
|
ENST00000481135.1:n.554A>G
|
|
|
ENST00000617432.4:c.-19A>G
|
ENSP00000477851.1:n.-19A>G
|
|
NM_001257197.1:c.1060A>G
|
NP_001244126.1:p.Arg354Gly
|
|
NM_001257198.1:c.1276A>G
|
NP_001244127.1:p.Arg426Gly
|
|
NM_003590.4:c.1258A>G
|
NP_003581.1:p.Arg420Gly
|
|
XM_006712800.2:c.1225A>G
|
XP_006712863.2:p.Arg409Gly
|
|
XM_011511994.1:c.1111A>G
|
XP_011510296.1:p.Arg371Gly
|
|
XM_011511995.1:c.1216A>G
|
XP_011510297.1:p.Arg406Gly
|
|
XM_011511996.1:c.1066A>G
|
XP_011510298.1:p.Arg356Gly
|
|
XM_011511997.1:c.958A>G
|
XP_011510299.1:p.Arg320Gly
|
|
XM_011511994.3:c.1111A>G
|
XP_011510296.1:p.Arg371Gly
|
|
XM_011511996.2:c.1066A>G
|
XP_011510298.1:p.Arg356Gly
|
|
NM_003590.5:c.1258A>G
MANE Select
|
NP_003581.1:p.Arg420Gly
|
|
NM_001257198.2:c.1276A>G
|
NP_001244127.1:p.Arg426Gly
|
|
NM_001257197.2:c.1060A>G
|
NP_001244126.1:p.Arg354Gly
|
|