ENST00000264640.9:c.*766G>A
|
ENSP00000466608.2:n.*766G>A
|
|
ENST00000348513.12:c.1204G>A
MANE Select
|
ENSP00000323967.6:p.Asp402Asn
|
|
ENST00000377808.9:c.*191G>A
|
ENSP00000367039.4:n.*191G>A
|
|
ENST00000400122.8:c.*191G>A
|
ENSP00000411607.2:n.*191G>A
|
|
ENST00000469334.6:n.1802G>A
|
|
|
ENST00000578044.6:c.994G>A
|
ENSP00000464511.1:p.Asp332Asn
|
|
ENST00000578112.6:c.*1001G>A
|
ENSP00000464501.1:n.*1001G>A
|
|
ENST00000580419.6:c.*183G>A
|
ENSP00000462475.2:n.*183G>A
|
|
ENST00000642576.1:n.2347G>A
|
|
|
ENST00000643030.1:n.1827G>A
|
|
|
ENST00000643255.1:c.*3268G>A
|
ENSP00000493957.1:n.*3268G>A
|
|
ENST00000643318.1:c.994G>A
|
ENSP00000494771.1:p.Asp332Asn
|
|
ENST00000643378.1:n.1759G>A
|
|
|
ENST00000643683.1:c.1204G>A
|
ENSP00000496094.1:p.Asp402Asn
|
|
ENST00000643893.1:n.1497G>A
|
|
|
ENST00000644443.1:n.3092G>A
|
|
|
ENST00000644523.1:n.1250G>A
|
|
|
ENST00000644527.1:c.976G>A
|
ENSP00000493974.1:p.Asp326Asn
|
|
ENST00000644701.1:c.*191G>A
|
ENSP00000496097.1:n.*191G>A
|
|
ENST00000644909.1:c.*473G>A
|
ENSP00000493649.1:n.*473G>A
|
|
ENST00000645152.1:n.1867G>A
|
|
|
ENST00000645227.1:c.*892G>A
|
ENSP00000495021.1:n.*892G>A
|
|
ENST00000646242.1:n.7116G>A
|
|
|
ENST00000646283.1:c.1012G>A
|
ENSP00000494537.1:p.Asp338Asn
|
|
ENST00000646401.1:n.2570G>A
|
|
|
ENST00000646448.1:n.2478G>A
|
|
|
ENST00000646856.1:c.*1080G>A
|
ENSP00000494505.1:n.*1080G>A
|
|
ENST00000647294.1:c.*1134G>A
|
ENSP00000494815.1:n.*1134G>A
|
|
ENST00000647508.1:c.1099G>A
|
ENSP00000496445.1:p.Asp367Asn
|
|
ENST00000647515.1:c.*735G>A
|
ENSP00000495857.1:n.*735G>A
|
|
ENST00000348513.10:c.1204G>A
|
ENSP00000323967.6:p.Asp402Asn
|
|
ENST00000377808.8:c.*191G>A
|
ENSP00000367039.4:n.*191G>A
|
|
ENST00000400122.7:c.*191G>A
|
ENSP00000411607.2:n.*191G>A
|
|
ENST00000431889.6:c.1150G>A
|
ENSP00000445370.1:p.Asp384Asn
|
|
ENST00000469334.5:n.1791G>A
|
|
|
ENST00000476049.1:c.*1552G>A
|
ENSP00000463483.1:n.*1552G>A
|
|
ENST00000578044.5:c.994G>A
|
ENSP00000464511.1:p.Asp332Asn
|
|
ENST00000578112.5:c.*1001G>A
|
ENSP00000464501.1:n.*1001G>A
|
|
ENST00000580419.5:c.1099G>A
|
ENSP00000462475.1:p.Asp367Asn
|
|
NM_003079.4:c.1204G>A
|
NP_003070.3:p.Asp402Asn
|
|
NM_003079.5:c.1204G>A
MANE Select
|
NP_003070.3:p.Asp402Asn
|
|