ENST00000638375.2:c.979T>G
|
ENSP00000492789.2:p.Ter327Gly
|
|
ENST00000706892.1:n.2805T>G
|
|
|
ENST00000706893.1:c.*80T>G
|
ENSP00000516609.1:n.*80T>G
|
|
ENST00000706894.1:c.*80T>G
|
ENSP00000516610.1:n.*80T>G
|
|
ENST00000706895.1:n.2085T>G
|
|
|
ENST00000706896.1:n.2392T>G
|
|
|
ENST00000706897.1:n.1814T>G
|
|
|
ENST00000706898.1:c.1114T>G
|
ENSP00000516611.1:p.Ter372Gly
|
|
ENST00000706899.1:n.1950T>G
|
|
|
ENST00000706900.1:c.1012T>G
|
ENSP00000516617.1:p.Ter338Gly
|
|
ENST00000706901.1:c.1096T>G
|
ENSP00000516612.1:p.Ter366Gly
|
|
ENST00000706902.1:c.1093+172T>G
|
ENSP00000516613.1:n.1093+172T>G
|
|
ENST00000706903.1:c.1096T>G
|
ENSP00000516614.1:p.Ter366Gly
|
|
ENST00000706904.1:c.1093+172T>G
|
ENSP00000516615.1:n.1093+172T>G
|
|
ENST00000706905.1:c.1096T>G
|
ENSP00000516616.1:p.Ter366Gly
|
|
ENST00000376809.10:c.1096T>G
MANE Select
|
ENSP00000366005.5:p.Ter366Gly
|
|
ENST00000376802.2:c.898T>G
|
ENSP00000365998.2:p.Ter300Gly
|
|
ENST00000376806.9:c.1114T>G
|
ENSP00000366002.5:p.Ter372Gly
|
|
ENST00000376809.9:c.1096T>G
|
ENSP00000366005.5:p.Ter366Gly
|
|
ENST00000396634.5:c.1096T>G
|
ENSP00000379873.1:p.Ter366Gly
|
|
ENST00000495183.5:n.1335T>G
|
|
|
ENST00000496081.5:n.1355T>G
|
|
|
NM_002116.7:c.1096T>G
|
NP_002107.3:p.Ter366Gly
|
|
NM_002116.8:c.1096T>G
MANE Select
|
NP_002107.3:p.Ter366Gly
|
|