ENST00000264640.9:c.*781G>A
|
ENSP00000466608.2:n.*781G>A
|
|
ENST00000348513.12:c.1219G>A
MANE Select
|
ENSP00000323967.6:p.Asp407Asn
|
|
ENST00000377808.9:c.*206G>A
|
ENSP00000367039.4:n.*206G>A
|
|
ENST00000400122.8:c.*206G>A
|
ENSP00000411607.2:n.*206G>A
|
|
ENST00000469334.6:n.1817G>A
|
|
|
ENST00000578044.6:c.1009G>A
|
ENSP00000464511.1:p.Asp337Asn
|
|
ENST00000578112.6:c.*1016G>A
|
ENSP00000464501.1:n.*1016G>A
|
|
ENST00000580419.6:c.*198G>A
|
ENSP00000462475.2:n.*198G>A
|
|
ENST00000642576.1:n.2362G>A
|
|
|
ENST00000643030.1:n.1842G>A
|
|
|
ENST00000643255.1:c.*3283G>A
|
ENSP00000493957.1:n.*3283G>A
|
|
ENST00000643318.1:c.1009G>A
|
ENSP00000494771.1:p.Asp337Asn
|
|
ENST00000643378.1:n.1774G>A
|
|
|
ENST00000643683.1:c.1219G>A
|
ENSP00000496094.1:p.Asp407Asn
|
|
ENST00000643893.1:n.1512G>A
|
|
|
ENST00000644443.1:n.3107G>A
|
|
|
ENST00000644523.1:n.1265G>A
|
|
|
ENST00000644527.1:c.991G>A
|
ENSP00000493974.1:p.Asp331Asn
|
|
ENST00000644701.1:c.*206G>A
|
ENSP00000496097.1:n.*206G>A
|
|
ENST00000644909.1:c.*488G>A
|
ENSP00000493649.1:n.*488G>A
|
|
ENST00000645152.1:n.1882G>A
|
|
|
ENST00000645227.1:c.*907G>A
|
ENSP00000495021.1:n.*907G>A
|
|
ENST00000646242.1:n.7131G>A
|
|
|
ENST00000646283.1:c.1027G>A
|
ENSP00000494537.1:p.Asp343Asn
|
|
ENST00000646401.1:n.2585G>A
|
|
|
ENST00000646448.1:n.2493G>A
|
|
|
ENST00000646856.1:c.*1095G>A
|
ENSP00000494505.1:n.*1095G>A
|
|
ENST00000647294.1:c.*1149G>A
|
ENSP00000494815.1:n.*1149G>A
|
|
ENST00000647508.1:c.1114G>A
|
ENSP00000496445.1:p.Asp372Asn
|
|
ENST00000647515.1:c.*750G>A
|
ENSP00000495857.1:n.*750G>A
|
|
ENST00000348513.10:c.1219G>A
|
ENSP00000323967.6:p.Asp407Asn
|
|
ENST00000377808.8:c.*206G>A
|
ENSP00000367039.4:n.*206G>A
|
|
ENST00000400122.7:c.*206G>A
|
ENSP00000411607.2:n.*206G>A
|
|
ENST00000431889.6:c.1165G>A
|
ENSP00000445370.1:p.Asp389Asn
|
|
ENST00000469334.5:n.1806G>A
|
|
|
ENST00000476049.1:c.*1567G>A
|
ENSP00000463483.1:n.*1567G>A
|
|
ENST00000578044.5:c.1009G>A
|
ENSP00000464511.1:p.Asp337Asn
|
|
ENST00000578112.5:c.*1016G>A
|
ENSP00000464501.1:n.*1016G>A
|
|
ENST00000580419.5:c.1114G>A
|
ENSP00000462475.1:p.Asp372Asn
|
|
NM_003079.4:c.1219G>A
|
NP_003070.3:p.Asp407Asn
|
|
NM_003079.5:c.1219G>A
MANE Select
|
NP_003070.3:p.Asp407Asn
|
|