ENST00000264640.9:c.*685G>A
|
ENSP00000466608.2:n.*685G>A
|
|
ENST00000348513.12:c.1123G>A
MANE Select
|
ENSP00000323967.6:p.Asp375Asn
|
|
ENST00000377808.9:c.*110G>A
|
ENSP00000367039.4:n.*110G>A
|
|
ENST00000400122.8:c.*110G>A
|
ENSP00000411607.2:n.*110G>A
|
|
ENST00000469334.6:n.1721G>A
|
|
|
ENST00000578044.6:c.913G>A
|
ENSP00000464511.1:p.Asp305Asn
|
|
ENST00000578112.6:c.*920G>A
|
ENSP00000464501.1:n.*920G>A
|
|
ENST00000580419.6:c.*102G>A
|
ENSP00000462475.2:n.*102G>A
|
|
ENST00000642576.1:n.2266G>A
|
|
|
ENST00000643030.1:n.1746G>A
|
|
|
ENST00000643255.1:c.*3187G>A
|
ENSP00000493957.1:n.*3187G>A
|
|
ENST00000643318.1:c.913G>A
|
ENSP00000494771.1:p.Asp305Asn
|
|
ENST00000643378.1:n.1678G>A
|
|
|
ENST00000643683.1:c.1123G>A
|
ENSP00000496094.1:p.Asp375Asn
|
|
ENST00000643893.1:n.1416G>A
|
|
|
ENST00000644443.1:n.3011G>A
|
|
|
ENST00000644523.1:n.1169G>A
|
|
|
ENST00000644527.1:c.895G>A
|
ENSP00000493974.1:p.Asp299Asn
|
|
ENST00000644701.1:c.*110G>A
|
ENSP00000496097.1:n.*110G>A
|
|
ENST00000644909.1:c.*392G>A
|
ENSP00000493649.1:n.*392G>A
|
|
ENST00000645152.1:n.1786G>A
|
|
|
ENST00000645227.1:c.*811G>A
|
ENSP00000495021.1:n.*811G>A
|
|
ENST00000646242.1:n.7035G>A
|
|
|
ENST00000646283.1:c.931G>A
|
ENSP00000494537.1:p.Asp311Asn
|
|
ENST00000646401.1:n.2489G>A
|
|
|
ENST00000646448.1:n.2397G>A
|
|
|
ENST00000646856.1:c.*999G>A
|
ENSP00000494505.1:n.*999G>A
|
|
ENST00000647294.1:c.*1053G>A
|
ENSP00000494815.1:n.*1053G>A
|
|
ENST00000647508.1:c.1018G>A
|
ENSP00000496445.1:p.Asp340Asn
|
|
ENST00000647515.1:c.*654G>A
|
ENSP00000495857.1:n.*654G>A
|
|
ENST00000348513.10:c.1123G>A
|
ENSP00000323967.6:p.Asp375Asn
|
|
ENST00000377808.8:c.*110G>A
|
ENSP00000367039.4:n.*110G>A
|
|
ENST00000400122.7:c.*110G>A
|
ENSP00000411607.2:n.*110G>A
|
|
ENST00000431889.6:c.1069G>A
|
ENSP00000445370.1:p.Asp357Asn
|
|
ENST00000469334.5:n.1710G>A
|
|
|
ENST00000476049.1:c.*1471G>A
|
ENSP00000463483.1:n.*1471G>A
|
|
ENST00000578044.5:c.913G>A
|
ENSP00000464511.1:p.Asp305Asn
|
|
ENST00000578112.5:c.*920G>A
|
ENSP00000464501.1:n.*920G>A
|
|
ENST00000580419.5:c.1018G>A
|
ENSP00000462475.1:p.Asp340Asn
|
|
NM_003079.4:c.1123G>A
|
NP_003070.3:p.Asp375Asn
|
|
NM_003079.5:c.1123G>A
MANE Select
|
NP_003070.3:p.Asp375Asn
|
|