ENST00000290866.10:c.3725G>A
MANE Select
|
ENSP00000290866.4:p.Arg1242His
|
|
ENST00000290863.10:c.2003G>A
|
ENSP00000290863.6:p.Arg668His
|
|
ENST00000290866.9:c.3725G>A
|
ENSP00000290866.4:p.Arg1242His
|
|
ENST00000413513.7:c.1880G>A
|
ENSP00000392247.3:p.Arg627His
|
|
ENST00000428043.5:c.*147G>A
|
ENSP00000397593.2:n.*147G>A
|
|
ENST00000577647.2:c.1969+185G>A
|
ENSP00000464149.1:n.1969+185G>A
|
|
ENST00000578839.5:c.*1480G>A
|
ENSP00000462110.2:n.*1480G>A
|
|
ENST00000579314.5:c.*1454G>A
|
ENSP00000462599.1:n.*1454G>A
|
|
NM_000789.3:c.3725G>A
|
NP_000780.1:p.Arg1242His
|
|
NM_001178057.1:c.1880G>A
|
NP_001171528.1:p.Arg627His
|
|
NM_152830.2:c.2003G>A
|
NP_690043.1:p.Arg668His
|
|
XM_005257110.1:c.3176G>A
|
XP_005257167.1:p.Arg1059His
|
|
XM_006721737.2:c.2063G>A
|
XP_006721800.2:p.Arg688His
|
|
XM_006721737.3:c.2063G>A
|
XP_006721800.2:p.Arg688His
|
|
NM_000789.4:c.3725G>A
MANE Select
|
NP_000780.1:p.Arg1242His
|
|
NM_001178057.2:c.1880G>A
|
NP_001171528.1:p.Arg627His
|
|
NM_152830.3:c.2003G>A
|
NP_690043.1:p.Arg668His
|
|
NM_001382700.1:c.3158G>A
|
NP_001369629.1:p.Arg1053His
|
|
NM_001382701.1:c.2873G>A
|
NP_001369630.1:p.Arg958His
|
|
NM_001382702.1:c.1340G>A
|
NP_001369631.1:p.Arg447His
|
|
NR_168483.1:n.2103G>A
|
|
|