ENST00000264640.9:c.*729G>C
|
ENSP00000466608.2:n.*729G>C
|
|
ENST00000348513.12:c.1167G>C
MANE Select
|
ENSP00000323967.6:p.Ser389=
|
|
ENST00000377808.9:c.*154G>C
|
ENSP00000367039.4:n.*154G>C
|
|
ENST00000400122.8:c.*154G>C
|
ENSP00000411607.2:n.*154G>C
|
|
ENST00000469334.6:n.1765G>C
|
|
|
ENST00000578044.6:c.957G>C
|
ENSP00000464511.1:p.Ser319=
|
|
ENST00000578112.6:c.*964G>C
|
ENSP00000464501.1:n.*964G>C
|
|
ENST00000580419.6:c.*146G>C
|
ENSP00000462475.2:n.*146G>C
|
|
ENST00000642576.1:n.2310G>C
|
|
|
ENST00000643030.1:n.1790G>C
|
|
|
ENST00000643255.1:c.*3231G>C
|
ENSP00000493957.1:n.*3231G>C
|
|
ENST00000643318.1:c.957G>C
|
ENSP00000494771.1:p.Ser319=
|
|
ENST00000643378.1:n.1722G>C
|
|
|
ENST00000643683.1:c.1167G>C
|
ENSP00000496094.1:p.Ser389=
|
|
ENST00000643893.1:n.1460G>C
|
|
|
ENST00000644443.1:n.3055G>C
|
|
|
ENST00000644523.1:n.1213G>C
|
|
|
ENST00000644527.1:c.939G>C
|
ENSP00000493974.1:p.Ser313=
|
|
ENST00000644701.1:c.*154G>C
|
ENSP00000496097.1:n.*154G>C
|
|
ENST00000644909.1:c.*436G>C
|
ENSP00000493649.1:n.*436G>C
|
|
ENST00000645152.1:n.1830G>C
|
|
|
ENST00000645227.1:c.*855G>C
|
ENSP00000495021.1:n.*855G>C
|
|
ENST00000646242.1:n.7079G>C
|
|
|
ENST00000646283.1:c.975G>C
|
ENSP00000494537.1:p.Ser325=
|
|
ENST00000646401.1:n.2533G>C
|
|
|
ENST00000646448.1:n.2441G>C
|
|
|
ENST00000646856.1:c.*1043G>C
|
ENSP00000494505.1:n.*1043G>C
|
|
ENST00000647294.1:c.*1097G>C
|
ENSP00000494815.1:n.*1097G>C
|
|
ENST00000647508.1:c.1062G>C
|
ENSP00000496445.1:p.Ser354=
|
|
ENST00000647515.1:c.*698G>C
|
ENSP00000495857.1:n.*698G>C
|
|
ENST00000348513.10:c.1167G>C
|
ENSP00000323967.6:p.Ser389=
|
|
ENST00000377808.8:c.*154G>C
|
ENSP00000367039.4:n.*154G>C
|
|
ENST00000400122.7:c.*154G>C
|
ENSP00000411607.2:n.*154G>C
|
|
ENST00000431889.6:c.1113G>C
|
ENSP00000445370.1:p.Ser371=
|
|
ENST00000469334.5:n.1754G>C
|
|
|
ENST00000476049.1:c.*1515G>C
|
ENSP00000463483.1:n.*1515G>C
|
|
ENST00000578044.5:c.957G>C
|
ENSP00000464511.1:p.Ser319=
|
|
ENST00000578112.5:c.*964G>C
|
ENSP00000464501.1:n.*964G>C
|
|
ENST00000580419.5:c.1062G>C
|
ENSP00000462475.1:p.Ser354=
|
|
NM_003079.4:c.1167G>C
|
NP_003070.3:p.Ser389=
|
|
NM_003079.5:c.1167G>C
MANE Select
|
NP_003070.3:p.Ser389=
|
|