ENST00000264640.9:c.*726C>T
|
ENSP00000466608.2:n.*726C>T
|
|
ENST00000348513.12:c.1164C>T
MANE Select
|
ENSP00000323967.6:p.Gly388=
|
|
ENST00000377808.9:c.*151C>T
|
ENSP00000367039.4:n.*151C>T
|
|
ENST00000400122.8:c.*151C>T
|
ENSP00000411607.2:n.*151C>T
|
|
ENST00000469334.6:n.1762C>T
|
|
|
ENST00000578044.6:c.954C>T
|
ENSP00000464511.1:p.Gly318=
|
|
ENST00000578112.6:c.*961C>T
|
ENSP00000464501.1:n.*961C>T
|
|
ENST00000580419.6:c.*143C>T
|
ENSP00000462475.2:n.*143C>T
|
|
ENST00000642576.1:n.2307C>T
|
|
|
ENST00000643030.1:n.1787C>T
|
|
|
ENST00000643255.1:c.*3228C>T
|
ENSP00000493957.1:n.*3228C>T
|
|
ENST00000643318.1:c.954C>T
|
ENSP00000494771.1:p.Gly318=
|
|
ENST00000643378.1:n.1719C>T
|
|
|
ENST00000643683.1:c.1164C>T
|
ENSP00000496094.1:p.Gly388=
|
|
ENST00000643893.1:n.1457C>T
|
|
|
ENST00000644443.1:n.3052C>T
|
|
|
ENST00000644523.1:n.1210C>T
|
|
|
ENST00000644527.1:c.936C>T
|
ENSP00000493974.1:p.Gly312=
|
|
ENST00000644701.1:c.*151C>T
|
ENSP00000496097.1:n.*151C>T
|
|
ENST00000644909.1:c.*433C>T
|
ENSP00000493649.1:n.*433C>T
|
|
ENST00000645152.1:n.1827C>T
|
|
|
ENST00000645227.1:c.*852C>T
|
ENSP00000495021.1:n.*852C>T
|
|
ENST00000646242.1:n.7076C>T
|
|
|
ENST00000646283.1:c.972C>T
|
ENSP00000494537.1:p.Gly324=
|
|
ENST00000646401.1:n.2530C>T
|
|
|
ENST00000646448.1:n.2438C>T
|
|
|
ENST00000646856.1:c.*1040C>T
|
ENSP00000494505.1:n.*1040C>T
|
|
ENST00000647294.1:c.*1094C>T
|
ENSP00000494815.1:n.*1094C>T
|
|
ENST00000647508.1:c.1059C>T
|
ENSP00000496445.1:p.Gly353=
|
|
ENST00000647515.1:c.*695C>T
|
ENSP00000495857.1:n.*695C>T
|
|
ENST00000348513.10:c.1164C>T
|
ENSP00000323967.6:p.Gly388=
|
|
ENST00000377808.8:c.*151C>T
|
ENSP00000367039.4:n.*151C>T
|
|
ENST00000400122.7:c.*151C>T
|
ENSP00000411607.2:n.*151C>T
|
|
ENST00000431889.6:c.1110C>T
|
ENSP00000445370.1:p.Gly370=
|
|
ENST00000469334.5:n.1751C>T
|
|
|
ENST00000476049.1:c.*1512C>T
|
ENSP00000463483.1:n.*1512C>T
|
|
ENST00000578044.5:c.954C>T
|
ENSP00000464511.1:p.Gly318=
|
|
ENST00000578112.5:c.*961C>T
|
ENSP00000464501.1:n.*961C>T
|
|
ENST00000580419.5:c.1059C>T
|
ENSP00000462475.1:p.Gly353=
|
|
NM_003079.4:c.1164C>T
|
NP_003070.3:p.Gly388=
|
|
NM_003079.5:c.1164C>T
MANE Select
|
NP_003070.3:p.Gly388=
|
|