ENST00000264640.9:c.*769C>A
|
ENSP00000466608.2:n.*769C>A
|
|
ENST00000348513.12:c.1207C>A
MANE Select
|
ENSP00000323967.6:p.Pro403Thr
|
|
ENST00000377808.9:c.*194C>A
|
ENSP00000367039.4:n.*194C>A
|
|
ENST00000400122.8:c.*194C>A
|
ENSP00000411607.2:n.*194C>A
|
|
ENST00000469334.6:n.1805C>A
|
|
|
ENST00000578044.6:c.997C>A
|
ENSP00000464511.1:p.Pro333Thr
|
|
ENST00000578112.6:c.*1004C>A
|
ENSP00000464501.1:n.*1004C>A
|
|
ENST00000580419.6:c.*186C>A
|
ENSP00000462475.2:n.*186C>A
|
|
ENST00000642576.1:n.2350C>A
|
|
|
ENST00000643030.1:n.1830C>A
|
|
|
ENST00000643255.1:c.*3271C>A
|
ENSP00000493957.1:n.*3271C>A
|
|
ENST00000643318.1:c.997C>A
|
ENSP00000494771.1:p.Pro333Thr
|
|
ENST00000643378.1:n.1762C>A
|
|
|
ENST00000643683.1:c.1207C>A
|
ENSP00000496094.1:p.Pro403Thr
|
|
ENST00000643893.1:n.1500C>A
|
|
|
ENST00000644443.1:n.3095C>A
|
|
|
ENST00000644523.1:n.1253C>A
|
|
|
ENST00000644527.1:c.979C>A
|
ENSP00000493974.1:p.Pro327Thr
|
|
ENST00000644701.1:c.*194C>A
|
ENSP00000496097.1:n.*194C>A
|
|
ENST00000644909.1:c.*476C>A
|
ENSP00000493649.1:n.*476C>A
|
|
ENST00000645152.1:n.1870C>A
|
|
|
ENST00000645227.1:c.*895C>A
|
ENSP00000495021.1:n.*895C>A
|
|
ENST00000646242.1:n.7119C>A
|
|
|
ENST00000646283.1:c.1015C>A
|
ENSP00000494537.1:p.Pro339Thr
|
|
ENST00000646401.1:n.2573C>A
|
|
|
ENST00000646448.1:n.2481C>A
|
|
|
ENST00000646856.1:c.*1083C>A
|
ENSP00000494505.1:n.*1083C>A
|
|
ENST00000647294.1:c.*1137C>A
|
ENSP00000494815.1:n.*1137C>A
|
|
ENST00000647508.1:c.1102C>A
|
ENSP00000496445.1:p.Pro368Thr
|
|
ENST00000647515.1:c.*738C>A
|
ENSP00000495857.1:n.*738C>A
|
|
ENST00000348513.10:c.1207C>A
|
ENSP00000323967.6:p.Pro403Thr
|
|
ENST00000377808.8:c.*194C>A
|
ENSP00000367039.4:n.*194C>A
|
|
ENST00000400122.7:c.*194C>A
|
ENSP00000411607.2:n.*194C>A
|
|
ENST00000431889.6:c.1153C>A
|
ENSP00000445370.1:p.Pro385Thr
|
|
ENST00000469334.5:n.1794C>A
|
|
|
ENST00000476049.1:c.*1555C>A
|
ENSP00000463483.1:n.*1555C>A
|
|
ENST00000578044.5:c.997C>A
|
ENSP00000464511.1:p.Pro333Thr
|
|
ENST00000578112.5:c.*1004C>A
|
ENSP00000464501.1:n.*1004C>A
|
|
ENST00000580419.5:c.1102C>A
|
ENSP00000462475.1:p.Pro368Thr
|
|
NM_003079.4:c.1207C>A
|
NP_003070.3:p.Pro403Thr
|
|
NM_003079.5:c.1207C>A
MANE Select
|
NP_003070.3:p.Pro403Thr
|
|