ENST00000264640.9:c.*1216G>T
|
ENSP00000466608.2:n.*1216G>T
|
|
ENST00000348513.12:c.*418G>T
MANE Select
|
ENSP00000323967.6:n.*418G>T
|
|
ENST00000377808.9:c.*641G>T
|
ENSP00000367039.4:n.*641G>T
|
|
ENST00000400122.8:c.*641G>T
|
ENSP00000411607.2:n.*641G>T
|
|
ENST00000469334.6:n.2252G>T
|
|
|
ENST00000578112.6:c.*1451G>T
|
ENSP00000464501.1:n.*1451G>T
|
|
ENST00000580419.6:c.*633G>T
|
ENSP00000462475.2:n.*633G>T
|
|
ENST00000642576.1:n.2797G>T
|
|
|
ENST00000643030.1:n.2277G>T
|
|
|
ENST00000643255.1:c.*3718G>T
|
ENSP00000493957.1:n.*3718G>T
|
|
ENST00000643318.1:c.*418G>T
|
ENSP00000494771.1:n.*418G>T
|
|
ENST00000643378.1:n.2209G>T
|
|
|
ENST00000643683.1:c.*418G>T
|
ENSP00000496094.1:n.*418G>T
|
|
ENST00000643893.1:n.1947G>T
|
|
|
ENST00000644443.1:n.3542G>T
|
|
|
ENST00000644523.1:n.1700G>T
|
|
|
ENST00000644527.1:c.*418G>T
|
ENSP00000493974.1:n.*418G>T
|
|
ENST00000644701.1:c.*641G>T
|
ENSP00000496097.1:n.*641G>T
|
|
ENST00000644909.1:c.*923G>T
|
ENSP00000493649.1:n.*923G>T
|
|
ENST00000645152.1:n.2317G>T
|
|
|
ENST00000645227.1:c.*1342G>T
|
ENSP00000495021.1:n.*1342G>T
|
|
ENST00000646242.1:n.7566G>T
|
|
|
ENST00000646283.1:c.*418G>T
|
ENSP00000494537.1:n.*418G>T
|
|
ENST00000646401.1:n.3020G>T
|
|
|
ENST00000646856.1:c.*1530G>T
|
ENSP00000494505.1:n.*1530G>T
|
|
ENST00000647294.1:c.*1584G>T
|
ENSP00000494815.1:n.*1584G>T
|
|
ENST00000647508.1:c.*418G>T
|
ENSP00000496445.1:n.*418G>T
|
|
ENST00000647515.1:c.*1185G>T
|
ENSP00000495857.1:n.*1185G>T
|
|
ENST00000348513.10:c.*418G>T
|
ENSP00000323967.6:n.*418G>T
|
|
ENST00000578112.5:c.*1451G>T
|
ENSP00000464501.1:n.*1451G>T
|
|
NM_003079.4:c.*418G>T
|
NP_003070.3:n.*418G>T
|
|
NM_003079.5:c.*418G>T
MANE Select
|
NP_003070.3:n.*418G>T
|
|