ENST00000290866.10:c.3835C>G
MANE Select
|
ENSP00000290866.4:p.Arg1279Gly
|
|
ENST00000290863.10:c.2113C>G
|
ENSP00000290863.6:p.Arg705Gly
|
|
ENST00000290866.9:c.3835C>G
|
ENSP00000290866.4:p.Arg1279Gly
|
|
ENST00000413513.7:c.1990C>G
|
ENSP00000392247.3:p.Arg664Gly
|
|
ENST00000428043.5:c.*257C>G
|
ENSP00000397593.2:n.*257C>G
|
|
ENST00000577647.2:c.1969+295C>G
|
ENSP00000464149.1:n.1969+295C>G
|
|
ENST00000578839.5:c.*1590C>G
|
ENSP00000462110.2:n.*1590C>G
|
|
ENST00000579314.5:c.*1564C>G
|
ENSP00000462599.1:n.*1564C>G
|
|
NM_000789.3:c.3835C>G
|
NP_000780.1:p.Arg1279Gly
|
|
NM_001178057.1:c.1990C>G
|
NP_001171528.1:p.Arg664Gly
|
|
NM_152830.2:c.2113C>G
|
NP_690043.1:p.Arg705Gly
|
|
XM_005257110.1:c.3286C>G
|
XP_005257167.1:p.Arg1096Gly
|
|
XM_006721737.2:c.2173C>G
|
XP_006721800.2:p.Arg725Gly
|
|
XM_006721737.3:c.2173C>G
|
XP_006721800.2:p.Arg725Gly
|
|
NM_000789.4:c.3835C>G
MANE Select
|
NP_000780.1:p.Arg1279Gly
|
|
NM_001178057.2:c.1990C>G
|
NP_001171528.1:p.Arg664Gly
|
|
NM_152830.3:c.2113C>G
|
NP_690043.1:p.Arg705Gly
|
|
NM_001382700.1:c.3268C>G
|
NP_001369629.1:p.Arg1090Gly
|
|
NM_001382701.1:c.2983C>G
|
NP_001369630.1:p.Arg995Gly
|
|
NM_001382702.1:c.1450C>G
|
NP_001369631.1:p.Arg484Gly
|
|
NR_168483.1:n.2213C>G
|
|
|