ENST00000290866.10:c.3858C>G
MANE Select
|
ENSP00000290866.4:p.Arg1286=
|
|
ENST00000290863.10:c.2136C>G
|
ENSP00000290863.6:p.Arg712=
|
|
ENST00000290866.9:c.3858C>G
|
ENSP00000290866.4:p.Arg1286=
|
|
ENST00000413513.7:c.2013C>G
|
ENSP00000392247.3:p.Arg671=
|
|
ENST00000428043.5:c.*280C>G
|
ENSP00000397593.2:n.*280C>G
|
|
ENST00000577647.2:c.1969+318C>G
|
ENSP00000464149.1:n.1969+318C>G
|
|
ENST00000578839.5:c.*1613C>G
|
ENSP00000462110.2:n.*1613C>G
|
|
ENST00000579314.5:c.*1587C>G
|
ENSP00000462599.1:n.*1587C>G
|
|
NM_000789.3:c.3858C>G
|
NP_000780.1:p.Arg1286=
|
|
NM_001178057.1:c.2013C>G
|
NP_001171528.1:p.Arg671=
|
|
NM_152830.2:c.2136C>G
|
NP_690043.1:p.Arg712=
|
|
XM_005257110.1:c.3309C>G
|
XP_005257167.1:p.Arg1103=
|
|
XM_006721737.2:c.2196C>G
|
XP_006721800.2:p.Arg732=
|
|
XM_006721737.3:c.2196C>G
|
XP_006721800.2:p.Arg732=
|
|
NM_000789.4:c.3858C>G
MANE Select
|
NP_000780.1:p.Arg1286=
|
|
NM_001178057.2:c.2013C>G
|
NP_001171528.1:p.Arg671=
|
|
NM_152830.3:c.2136C>G
|
NP_690043.1:p.Arg712=
|
|
NM_001382700.1:c.3291C>G
|
NP_001369629.1:p.Arg1097=
|
|
NM_001382701.1:c.3006C>G
|
NP_001369630.1:p.Arg1002=
|
|
NM_001382702.1:c.1473C>G
|
NP_001369631.1:p.Arg491=
|
|
NR_168483.1:n.2236C>G
|
|
|