ENST00000290866.10:c.3857G>A
MANE Select
|
ENSP00000290866.4:p.Arg1286His
|
|
ENST00000290863.10:c.2135G>A
|
ENSP00000290863.6:p.Arg712His
|
|
ENST00000290866.9:c.3857G>A
|
ENSP00000290866.4:p.Arg1286His
|
|
ENST00000413513.7:c.2012G>A
|
ENSP00000392247.3:p.Arg671His
|
|
ENST00000428043.5:c.*279G>A
|
ENSP00000397593.2:n.*279G>A
|
|
ENST00000577647.2:c.1969+317G>A
|
ENSP00000464149.1:n.1969+317G>A
|
|
ENST00000578839.5:c.*1612G>A
|
ENSP00000462110.2:n.*1612G>A
|
|
ENST00000579314.5:c.*1586G>A
|
ENSP00000462599.1:n.*1586G>A
|
|
NM_000789.3:c.3857G>A
|
NP_000780.1:p.Arg1286His
|
|
NM_001178057.1:c.2012G>A
|
NP_001171528.1:p.Arg671His
|
|
NM_152830.2:c.2135G>A
|
NP_690043.1:p.Arg712His
|
|
XM_005257110.1:c.3308G>A
|
XP_005257167.1:p.Arg1103His
|
|
XM_006721737.2:c.2195G>A
|
XP_006721800.2:p.Arg732His
|
|
XM_006721737.3:c.2195G>A
|
XP_006721800.2:p.Arg732His
|
|
NM_000789.4:c.3857G>A
MANE Select
|
NP_000780.1:p.Arg1286His
|
|
NM_001178057.2:c.2012G>A
|
NP_001171528.1:p.Arg671His
|
|
NM_152830.3:c.2135G>A
|
NP_690043.1:p.Arg712His
|
|
NM_001382700.1:c.3290G>A
|
NP_001369629.1:p.Arg1097His
|
|
NM_001382701.1:c.3005G>A
|
NP_001369630.1:p.Arg1002His
|
|
NM_001382702.1:c.1472G>A
|
NP_001369631.1:p.Arg491His
|
|
NR_168483.1:n.2235G>A
|
|
|