ENST00000638375.2:c.895+228G>T
|
ENSP00000492789.2:n.895+228G>T
|
|
ENST00000706892.1:n.1977G>T
|
|
|
ENST00000706893.1:c.1055G>T
|
ENSP00000516609.1:p.Arg352Met
|
|
ENST00000706894.1:c.1012+9G>T
|
ENSP00000516610.1:n.1012+9G>T
|
|
ENST00000706895.1:n.1399G>T
|
|
|
ENST00000706896.1:n.1875G>T
|
|
|
ENST00000706897.1:n.1297G>T
|
|
|
ENST00000706898.1:c.1021G>T
|
ENSP00000516611.1:p.Gly341Trp
|
|
ENST00000706899.1:n.1866+9G>T
|
|
|
ENST00000706900.1:c.928+9G>T
|
ENSP00000516617.1:n.928+9G>T
|
|
ENST00000706901.1:c.1012+9G>T
|
ENSP00000516612.1:n.1012+9G>T
|
|
ENST00000706902.1:c.1012+9G>T
|
ENSP00000516613.1:n.1012+9G>T
|
|
ENST00000706903.1:c.1012+9G>T
|
ENSP00000516614.1:n.1012+9G>T
|
|
ENST00000706904.1:c.1012+9G>T
|
ENSP00000516615.1:n.1012+9G>T
|
|
ENST00000706905.1:c.1012+9G>T
|
ENSP00000516616.1:n.1012+9G>T
|
|
ENST00000376809.10:c.1012+9G>T
MANE Select
|
ENSP00000366005.5:n.1012+9G>T
|
|
ENST00000638375.1:c.895+228G>T
|
ENSP00000492789.1:n.895+228G>T
|
|
ENST00000376802.2:c.895+228G>T
|
ENSP00000365998.2:n.895+228G>T
|
|
ENST00000376806.9:c.1021G>T
|
ENSP00000366002.5:p.Gly341Trp
|
|
ENST00000376809.9:c.1012+9G>T
|
ENSP00000366005.5:n.1012+9G>T
|
|
ENST00000396634.5:c.1012+9G>T
|
ENSP00000379873.1:n.1012+9G>T
|
|
ENST00000461903.1:n.1262G>T
|
|
|
ENST00000479320.5:n.1253+9G>T
|
|
|
ENST00000495183.5:n.1255+9G>T
|
|
|
ENST00000496081.5:n.838G>T
|
|
|
NM_002116.7:c.1012+9G>T
|
NP_002107.3:n.1012+9G>T
|
|
NM_002116.8:c.1012+9G>T
MANE Select
|
NP_002107.3:n.1012+9G>T
|
|