|
ENST00000264640.9:c.*874G>A
|
ENSP00000466608.2:n.*874G>A
|
|
|
ENST00000348513.12:c.*76G>A
MANE Select
|
ENSP00000323967.6:n.*76G>A
|
|
|
ENST00000377808.9:c.*299G>A
|
ENSP00000367039.4:n.*299G>A
|
|
|
ENST00000400122.8:c.*299G>A
|
ENSP00000411607.2:n.*299G>A
|
|
|
ENST00000469334.6:n.1910G>A
|
|
|
|
ENST00000578112.6:c.*1109G>A
|
ENSP00000464501.1:n.*1109G>A
|
|
|
ENST00000580419.6:c.*291G>A
|
ENSP00000462475.2:n.*291G>A
|
|
|
ENST00000642576.1:n.2455G>A
|
|
|
|
ENST00000643030.1:n.1935G>A
|
|
|
|
ENST00000643255.1:c.*3376G>A
|
ENSP00000493957.1:n.*3376G>A
|
|
|
ENST00000643318.1:c.*76G>A
|
ENSP00000494771.1:n.*76G>A
|
|
|
ENST00000643378.1:n.1867G>A
|
|
|
|
ENST00000643683.1:c.*76G>A
|
ENSP00000496094.1:n.*76G>A
|
|
|
ENST00000643893.1:n.1605G>A
|
|
|
|
ENST00000644443.1:n.3200G>A
|
|
|
|
ENST00000644523.1:n.1358G>A
|
|
|
|
ENST00000644527.1:c.*76G>A
|
ENSP00000493974.1:n.*76G>A
|
|
|
ENST00000644701.1:c.*299G>A
|
ENSP00000496097.1:n.*299G>A
|
|
|
ENST00000644909.1:c.*581G>A
|
ENSP00000493649.1:n.*581G>A
|
|
|
ENST00000645152.1:n.1975G>A
|
|
|
|
ENST00000645227.1:c.*1000G>A
|
ENSP00000495021.1:n.*1000G>A
|
|
|
ENST00000646242.1:n.7224G>A
|
|
|
|
ENST00000646283.1:c.*76G>A
|
ENSP00000494537.1:n.*76G>A
|
|
|
ENST00000646401.1:n.2678G>A
|
|
|
|
ENST00000646856.1:c.*1188G>A
|
ENSP00000494505.1:n.*1188G>A
|
|
|
ENST00000647294.1:c.*1242G>A
|
ENSP00000494815.1:n.*1242G>A
|
|
|
ENST00000647508.1:c.*76G>A
|
ENSP00000496445.1:n.*76G>A
|
|
|
ENST00000647515.1:c.*843G>A
|
ENSP00000495857.1:n.*843G>A
|
|
|
ENST00000348513.10:c.*76G>A
|
ENSP00000323967.6:n.*76G>A
|
|
|
ENST00000431889.6:c.*76G>A
|
ENSP00000445370.1:n.*76G>A
|
|
|
ENST00000469334.5:n.1899G>A
|
|
|
|
ENST00000578112.5:c.*1109G>A
|
ENSP00000464501.1:n.*1109G>A
|
|
|
NM_003079.4:c.*76G>A
|
NP_003070.3:n.*76G>A
|
|
|
NM_003079.5:c.*76G>A
MANE Select
|
NP_003070.3:n.*76G>A
|
|
