ENST00000290866.10:c.3836G>A
MANE Select
|
ENSP00000290866.4:p.Arg1279Gln
|
|
ENST00000290863.10:c.2114G>A
|
ENSP00000290863.6:p.Arg705Gln
|
|
ENST00000290866.9:c.3836G>A
|
ENSP00000290866.4:p.Arg1279Gln
|
|
ENST00000413513.7:c.1991G>A
|
ENSP00000392247.3:p.Arg664Gln
|
|
ENST00000428043.5:c.*258G>A
|
ENSP00000397593.2:n.*258G>A
|
|
ENST00000577647.2:c.1969+296G>A
|
ENSP00000464149.1:n.1969+296G>A
|
|
ENST00000578839.5:c.*1591G>A
|
ENSP00000462110.2:n.*1591G>A
|
|
ENST00000579314.5:c.*1565G>A
|
ENSP00000462599.1:n.*1565G>A
|
|
NM_000789.3:c.3836G>A
|
NP_000780.1:p.Arg1279Gln
|
|
NM_001178057.1:c.1991G>A
|
NP_001171528.1:p.Arg664Gln
|
|
NM_152830.2:c.2114G>A
|
NP_690043.1:p.Arg705Gln
|
|
XM_005257110.1:c.3287G>A
|
XP_005257167.1:p.Arg1096Gln
|
|
XM_006721737.2:c.2174G>A
|
XP_006721800.2:p.Arg725Gln
|
|
XM_006721737.3:c.2174G>A
|
XP_006721800.2:p.Arg725Gln
|
|
NM_000789.4:c.3836G>A
MANE Select
|
NP_000780.1:p.Arg1279Gln
|
|
NM_001178057.2:c.1991G>A
|
NP_001171528.1:p.Arg664Gln
|
|
NM_152830.3:c.2114G>A
|
NP_690043.1:p.Arg705Gln
|
|
NM_001382700.1:c.3269G>A
|
NP_001369629.1:p.Arg1090Gln
|
|
NM_001382701.1:c.2984G>A
|
NP_001369630.1:p.Arg995Gln
|
|
NM_001382702.1:c.1451G>A
|
NP_001369631.1:p.Arg484Gln
|
|
NR_168483.1:n.2214G>A
|
|
|