ENST00000290866.10:c.3851G>A
MANE Select
|
ENSP00000290866.4:p.Arg1284His
|
|
ENST00000290863.10:c.2129G>A
|
ENSP00000290863.6:p.Arg710His
|
|
ENST00000290866.9:c.3851G>A
|
ENSP00000290866.4:p.Arg1284His
|
|
ENST00000413513.7:c.2006G>A
|
ENSP00000392247.3:p.Arg669His
|
|
ENST00000428043.5:c.*273G>A
|
ENSP00000397593.2:n.*273G>A
|
|
ENST00000577647.2:c.1969+311G>A
|
ENSP00000464149.1:n.1969+311G>A
|
|
ENST00000578839.5:c.*1606G>A
|
ENSP00000462110.2:n.*1606G>A
|
|
ENST00000579314.5:c.*1580G>A
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ENSP00000462599.1:n.*1580G>A
|
|
NM_000789.3:c.3851G>A
|
NP_000780.1:p.Arg1284His
|
|
NM_001178057.1:c.2006G>A
|
NP_001171528.1:p.Arg669His
|
|
NM_152830.2:c.2129G>A
|
NP_690043.1:p.Arg710His
|
|
XM_005257110.1:c.3302G>A
|
XP_005257167.1:p.Arg1101His
|
|
XM_006721737.2:c.2189G>A
|
XP_006721800.2:p.Arg730His
|
|
XM_006721737.3:c.2189G>A
|
XP_006721800.2:p.Arg730His
|
|
NM_000789.4:c.3851G>A
MANE Select
|
NP_000780.1:p.Arg1284His
|
|
NM_001178057.2:c.2006G>A
|
NP_001171528.1:p.Arg669His
|
|
NM_152830.3:c.2129G>A
|
NP_690043.1:p.Arg710His
|
|
NM_001382700.1:c.3284G>A
|
NP_001369629.1:p.Arg1095His
|
|
NM_001382701.1:c.2999G>A
|
NP_001369630.1:p.Arg1000His
|
|
NM_001382702.1:c.1466G>A
|
NP_001369631.1:p.Arg489His
|
|
NR_168483.1:n.2229G>A
|
|
|