ENST00000470050.2:c.1336G>T
|
ENSP00000515580.1:p.Glu446Ter
|
|
ENST00000703945.1:c.1252G>T
|
ENSP00000515578.1:p.Glu418Ter
|
|
ENST00000703946.1:c.1265+2462G>T
|
ENSP00000515579.1:n.1265+2462G>T
|
|
ENST00000703947.1:c.946G>T
|
ENSP00000515581.1:p.Glu316Ter
|
|
ENST00000703948.1:c.*953G>T
|
ENSP00000515582.1:n.*953G>T
|
|
ENST00000703949.1:c.1336G>T
|
ENSP00000515583.1:p.Glu446Ter
|
|
ENST00000703950.1:c.1336G>T
|
ENSP00000515584.1:p.Glu446Ter
|
|
ENST00000703951.1:c.1265+2462G>T
|
ENSP00000515585.1:n.1265+2462G>T
|
|
ENST00000703952.1:c.1265+2462G>T
|
ENSP00000515586.1:n.1265+2462G>T
|
|
ENST00000703953.1:c.*599G>T
|
ENSP00000515587.1:n.*599G>T
|
|
ENST00000703954.1:c.1216G>T
|
ENSP00000515588.1:p.Glu406Ter
|
|
ENST00000703955.1:n.1886G>T
|
|
|
ENST00000298649.8:c.1333G>T
|
ENSP00000298649.3:p.Glu445Ter
|
|
ENST00000359426.7:c.1336G>T
MANE Select
|
ENSP00000352398.6:p.Glu446Ter
|
|
ENST00000436817.6:c.1348G>T
|
ENSP00000415949.2:p.Glu450Ter
|
|
ENST00000493591.6:c.*1224G>T
|
ENSP00000494917.1:n.*1224G>T
|
|
ENST00000643399.2:c.1348G>T
MANE Plus Clinical
|
ENSP00000494664.1:p.Glu450Ter
|
|
ENST00000298649.7:c.1333G>T
|
ENSP00000298649.3:p.Glu445Ter
|
|
ENST00000359426.6:c.1336G>T
|
ENSP00000352398.6:p.Glu446Ter
|
|
ENST00000360289.6:c.1300G>T
|
ENSP00000353433.2:p.Glu434Ter
|
|
ENST00000448642.6:c.1348G>T
|
ENSP00000402103.3:p.Glu450Ter
|
|
ENST00000494253.1:n.1562G>T
|
|
|
NM_000188.2:c.1336G>T
|
NP_000179.2:p.Glu446Ter
|
|
NM_033496.2:c.1333G>T
|
NP_277031.1:p.Glu445Ter
|
|
NM_033497.2:c.1348G>T
|
NP_277032.1:p.Glu450Ter
|
|
NM_033498.2:c.1348G>T
|
NP_277033.1:p.Glu450Ter
|
|
NM_033500.2:c.1300G>T , LRG_365t1:c.1300G>T
|
NP_277035.2:p.Glu434Ter
|
|
XM_005269735.2:c.1465G>T
|
XP_005269792.1:p.Glu489Ter
|
|
XM_005269736.1:c.1348G>T
|
XP_005269793.1:p.Glu450Ter
|
|
XM_005269737.1:c.1252G>T
|
XP_005269794.1:p.Glu418Ter
|
|
XM_011539732.1:c.1300G>T
|
XP_011538034.1:p.Glu434Ter
|
|
XM_011539733.1:c.1294G>T
|
XP_011538035.1:p.Glu432Ter
|
|
XM_011539734.1:c.1291G>T
|
XP_011538036.1:p.Glu431Ter
|
|
NM_001322364.1:c.1348G>T
|
NP_001309293.1:p.Glu450Ter
|
|
NM_001322365.1:c.1441G>T
|
NP_001309294.1:p.Glu481Ter
|
|
NM_001322366.1:c.1252G>T
|
NP_001309295.1:p.Glu418Ter
|
|
NM_001322367.1:c.1240G>T
|
NP_001309296.1:p.Glu414Ter
|
|
NM_001358263.1:c.1348G>T
MANE Plus Clinical
|
NP_001345192.1:p.Glu450Ter
|
|
XM_024447969.1:c.1348G>T
|
XP_024303737.1:p.Glu450Ter
|
|
NM_000188.3:c.1336G>T
MANE Select
|
NP_000179.2:p.Glu446Ter
|
|
NM_001322364.2:c.1348G>T
|
NP_001309293.1:p.Glu450Ter
|
|
NM_001322365.2:c.1441G>T
|
NP_001309294.1:p.Glu481Ter
|
|
NM_033496.3:c.1333G>T
|
NP_277031.1:p.Glu445Ter
|
|
NM_033497.3:c.1348G>T
|
NP_277032.1:p.Glu450Ter
|
|
NM_033498.3:c.1348G>T
|
NP_277033.1:p.Glu450Ter
|
|