ENST00000264640.9:c.*1080T>G
|
ENSP00000466608.2:n.*1080T>G
|
|
ENST00000348513.12:c.*282T>G
MANE Select
|
ENSP00000323967.6:n.*282T>G
|
|
ENST00000377808.9:c.*505T>G
|
ENSP00000367039.4:n.*505T>G
|
|
ENST00000400122.8:c.*505T>G
|
ENSP00000411607.2:n.*505T>G
|
|
ENST00000469334.6:n.2116T>G
|
|
|
ENST00000578112.6:c.*1315T>G
|
ENSP00000464501.1:n.*1315T>G
|
|
ENST00000580419.6:c.*497T>G
|
ENSP00000462475.2:n.*497T>G
|
|
ENST00000642576.1:n.2661T>G
|
|
|
ENST00000643030.1:n.2141T>G
|
|
|
ENST00000643255.1:c.*3582T>G
|
ENSP00000493957.1:n.*3582T>G
|
|
ENST00000643318.1:c.*282T>G
|
ENSP00000494771.1:n.*282T>G
|
|
ENST00000643378.1:n.2073T>G
|
|
|
ENST00000643683.1:c.*282T>G
|
ENSP00000496094.1:n.*282T>G
|
|
ENST00000643893.1:n.1811T>G
|
|
|
ENST00000644443.1:n.3406T>G
|
|
|
ENST00000644523.1:n.1564T>G
|
|
|
ENST00000644527.1:c.*282T>G
|
ENSP00000493974.1:n.*282T>G
|
|
ENST00000644701.1:c.*505T>G
|
ENSP00000496097.1:n.*505T>G
|
|
ENST00000644909.1:c.*787T>G
|
ENSP00000493649.1:n.*787T>G
|
|
ENST00000645152.1:n.2181T>G
|
|
|
ENST00000645227.1:c.*1206T>G
|
ENSP00000495021.1:n.*1206T>G
|
|
ENST00000646242.1:n.7430T>G
|
|
|
ENST00000646283.1:c.*282T>G
|
ENSP00000494537.1:n.*282T>G
|
|
ENST00000646401.1:n.2884T>G
|
|
|
ENST00000646856.1:c.*1394T>G
|
ENSP00000494505.1:n.*1394T>G
|
|
ENST00000647294.1:c.*1448T>G
|
ENSP00000494815.1:n.*1448T>G
|
|
ENST00000647508.1:c.*282T>G
|
ENSP00000496445.1:n.*282T>G
|
|
ENST00000647515.1:c.*1049T>G
|
ENSP00000495857.1:n.*1049T>G
|
|
ENST00000348513.10:c.*282T>G
|
ENSP00000323967.6:n.*282T>G
|
|
ENST00000431889.6:c.*282T>G
|
ENSP00000445370.1:n.*282T>G
|
|
ENST00000469334.5:n.2105T>G
|
|
|
ENST00000578112.5:c.*1315T>G
|
ENSP00000464501.1:n.*1315T>G
|
|
NM_003079.4:c.*282T>G
|
NP_003070.3:n.*282T>G
|
|
NM_003079.5:c.*282T>G
MANE Select
|
NP_003070.3:n.*282T>G
|
|