ENST00000638375.2:c.1171G>T
|
ENSP00000492789.2:n.1171G>T
|
|
ENST00000706892.1:n.2997G>T
|
|
|
ENST00000706893.1:c.*272G>T
|
ENSP00000516609.1:n.*272G>T
|
|
ENST00000706894.1:c.*272G>T
|
ENSP00000516610.1:n.*272G>T
|
|
ENST00000706895.1:n.2277G>T
|
|
|
ENST00000706896.1:n.2584G>T
|
|
|
ENST00000706897.1:n.2006G>T
|
|
|
ENST00000706898.1:c.*190G>T
|
ENSP00000516611.1:n.*190G>T
|
|
ENST00000706899.1:n.2142G>T
|
|
|
ENST00000706900.1:c.*190G>T
|
ENSP00000516617.1:n.*190G>T
|
|
ENST00000706901.1:c.*190G>T
|
ENSP00000516612.1:n.*190G>T
|
|
ENST00000706902.1:c.1093+364G>T
|
ENSP00000516613.1:n.1093+364G>T
|
|
ENST00000706903.1:c.*124+66G>T
|
ENSP00000516614.1:n.*124+66G>T
|
|
ENST00000706904.1:c.1093+364G>T
|
ENSP00000516615.1:n.1093+364G>T
|
|
ENST00000706905.1:c.*190G>T
|
ENSP00000516616.1:n.*190G>T
|
|
ENST00000376809.10:c.*190G>T
MANE Select
|
ENSP00000366005.5:n.*190G>T
|
|
ENST00000376802.2:c.*190G>T
|
ENSP00000365998.2:n.*190G>T
|
|
ENST00000376806.9:c.*190G>T
|
ENSP00000366002.5:n.*190G>T
|
|
ENST00000376809.9:c.*190G>T
|
ENSP00000366005.5:n.*190G>T
|
|
ENST00000396634.5:c.*190G>T
|
ENSP00000379873.1:n.*190G>T
|
|
ENST00000495183.5:n.1527G>T
|
|
|
ENST00000496081.5:n.1547G>T
|
|
|
NM_002116.7:c.*190G>T
|
NP_002107.3:n.*190G>T
|
|
NM_002116.8:c.*190G>T
MANE Select
|
NP_002107.3:n.*190G>T
|
|