ENST00000264640.9:c.*724G>C
|
ENSP00000466608.2:n.*724G>C
|
|
ENST00000348513.12:c.1162G>C
MANE Select
|
ENSP00000323967.6:p.Gly388Arg
|
|
ENST00000377808.9:c.*149G>C
|
ENSP00000367039.4:n.*149G>C
|
|
ENST00000400122.8:c.*149G>C
|
ENSP00000411607.2:n.*149G>C
|
|
ENST00000469334.6:n.1760G>C
|
|
|
ENST00000578044.6:c.952G>C
|
ENSP00000464511.1:p.Gly318Arg
|
|
ENST00000578112.6:c.*959G>C
|
ENSP00000464501.1:n.*959G>C
|
|
ENST00000580419.6:c.*141G>C
|
ENSP00000462475.2:n.*141G>C
|
|
ENST00000642576.1:n.2305G>C
|
|
|
ENST00000643030.1:n.1785G>C
|
|
|
ENST00000643255.1:c.*3226G>C
|
ENSP00000493957.1:n.*3226G>C
|
|
ENST00000643318.1:c.952G>C
|
ENSP00000494771.1:p.Gly318Arg
|
|
ENST00000643378.1:n.1717G>C
|
|
|
ENST00000643683.1:c.1162G>C
|
ENSP00000496094.1:p.Gly388Arg
|
|
ENST00000643893.1:n.1455G>C
|
|
|
ENST00000644443.1:n.3050G>C
|
|
|
ENST00000644523.1:n.1208G>C
|
|
|
ENST00000644527.1:c.934G>C
|
ENSP00000493974.1:p.Gly312Arg
|
|
ENST00000644701.1:c.*149G>C
|
ENSP00000496097.1:n.*149G>C
|
|
ENST00000644909.1:c.*431G>C
|
ENSP00000493649.1:n.*431G>C
|
|
ENST00000645152.1:n.1825G>C
|
|
|
ENST00000645227.1:c.*850G>C
|
ENSP00000495021.1:n.*850G>C
|
|
ENST00000646242.1:n.7074G>C
|
|
|
ENST00000646283.1:c.970G>C
|
ENSP00000494537.1:p.Gly324Arg
|
|
ENST00000646401.1:n.2528G>C
|
|
|
ENST00000646448.1:n.2436G>C
|
|
|
ENST00000646856.1:c.*1038G>C
|
ENSP00000494505.1:n.*1038G>C
|
|
ENST00000647294.1:c.*1092G>C
|
ENSP00000494815.1:n.*1092G>C
|
|
ENST00000647508.1:c.1057G>C
|
ENSP00000496445.1:p.Gly353Arg
|
|
ENST00000647515.1:c.*693G>C
|
ENSP00000495857.1:n.*693G>C
|
|
ENST00000348513.10:c.1162G>C
|
ENSP00000323967.6:p.Gly388Arg
|
|
ENST00000377808.8:c.*149G>C
|
ENSP00000367039.4:n.*149G>C
|
|
ENST00000400122.7:c.*149G>C
|
ENSP00000411607.2:n.*149G>C
|
|
ENST00000431889.6:c.1108G>C
|
ENSP00000445370.1:p.Gly370Arg
|
|
ENST00000469334.5:n.1749G>C
|
|
|
ENST00000476049.1:c.*1510G>C
|
ENSP00000463483.1:n.*1510G>C
|
|
ENST00000578044.5:c.952G>C
|
ENSP00000464511.1:p.Gly318Arg
|
|
ENST00000578112.5:c.*959G>C
|
ENSP00000464501.1:n.*959G>C
|
|
ENST00000580419.5:c.1057G>C
|
ENSP00000462475.1:p.Gly353Arg
|
|
NM_003079.4:c.1162G>C
|
NP_003070.3:p.Gly388Arg
|
|
NM_003079.5:c.1162G>C
MANE Select
|
NP_003070.3:p.Gly388Arg
|
|