ENST00000264640.9:c.*1134G>T
|
ENSP00000466608.2:n.*1134G>T
|
|
ENST00000348513.12:c.*336G>T
MANE Select
|
ENSP00000323967.6:n.*336G>T
|
|
ENST00000377808.9:c.*559G>T
|
ENSP00000367039.4:n.*559G>T
|
|
ENST00000400122.8:c.*559G>T
|
ENSP00000411607.2:n.*559G>T
|
|
ENST00000469334.6:n.2170G>T
|
|
|
ENST00000578112.6:c.*1369G>T
|
ENSP00000464501.1:n.*1369G>T
|
|
ENST00000580419.6:c.*551G>T
|
ENSP00000462475.2:n.*551G>T
|
|
ENST00000642576.1:n.2715G>T
|
|
|
ENST00000643030.1:n.2195G>T
|
|
|
ENST00000643255.1:c.*3636G>T
|
ENSP00000493957.1:n.*3636G>T
|
|
ENST00000643318.1:c.*336G>T
|
ENSP00000494771.1:n.*336G>T
|
|
ENST00000643378.1:n.2127G>T
|
|
|
ENST00000643683.1:c.*336G>T
|
ENSP00000496094.1:n.*336G>T
|
|
ENST00000643893.1:n.1865G>T
|
|
|
ENST00000644443.1:n.3460G>T
|
|
|
ENST00000644523.1:n.1618G>T
|
|
|
ENST00000644527.1:c.*336G>T
|
ENSP00000493974.1:n.*336G>T
|
|
ENST00000644701.1:c.*559G>T
|
ENSP00000496097.1:n.*559G>T
|
|
ENST00000644909.1:c.*841G>T
|
ENSP00000493649.1:n.*841G>T
|
|
ENST00000645152.1:n.2235G>T
|
|
|
ENST00000645227.1:c.*1260G>T
|
ENSP00000495021.1:n.*1260G>T
|
|
ENST00000646242.1:n.7484G>T
|
|
|
ENST00000646283.1:c.*336G>T
|
ENSP00000494537.1:n.*336G>T
|
|
ENST00000646401.1:n.2938G>T
|
|
|
ENST00000646856.1:c.*1448G>T
|
ENSP00000494505.1:n.*1448G>T
|
|
ENST00000647294.1:c.*1502G>T
|
ENSP00000494815.1:n.*1502G>T
|
|
ENST00000647508.1:c.*336G>T
|
ENSP00000496445.1:n.*336G>T
|
|
ENST00000647515.1:c.*1103G>T
|
ENSP00000495857.1:n.*1103G>T
|
|
ENST00000348513.10:c.*336G>T
|
ENSP00000323967.6:n.*336G>T
|
|
ENST00000578112.5:c.*1369G>T
|
ENSP00000464501.1:n.*1369G>T
|
|
NM_003079.4:c.*336G>T
|
NP_003070.3:n.*336G>T
|
|
NM_003079.5:c.*336G>T
MANE Select
|
NP_003070.3:n.*336G>T
|
|