ENST00000695850.1:n.785G>T
|
|
|
ENST00000695853.1:c.*668G>T
|
ENSP00000512218.1:n.*668G>T
|
|
ENST00000423902.7:c.7609G>T
MANE Select
|
ENSP00000392028.1:p.Glu2537Ter
|
|
ENST00000423902.6:c.7609G>T
|
ENSP00000392028.1:p.Glu2537Ter
|
|
ENST00000524602.5:c.1717-1325G>T
|
ENSP00000437061.1:n.1717-1325G>T
|
|
ENST00000531695.1:n.33G>T
|
|
|
ENST00000618450.1:n.1G>T
|
|
|
NM_001316690.1:c.1717-1325G>T
|
NP_001303619.1:n.1717-1325G>T
|
|
NM_017780.3:c.7609G>T
|
NP_060250.2:p.Glu2537Ter
|
|
XM_011517553.1:c.7699G>T
|
XP_011515855.1:p.Glu2567Ter
|
|
XM_011517554.1:c.7699G>T
|
XP_011515856.1:p.Glu2567Ter
|
|
XM_011517555.1:c.7696G>T
|
XP_011515857.1:p.Glu2566Ter
|
|
XM_011517556.1:c.7699-1292G>T
|
XP_011515858.1:n.7699-1292G>T
|
|
XM_011517557.1:c.5686G>T
|
XP_011515859.1:p.Glu1896Ter
|
|
XM_011517558.1:c.5236G>T
|
XP_011515860.1:p.Glu1746Ter
|
|
XM_011517559.1:c.4444G>T
|
XP_011515861.1:p.Glu1482Ter
|
|
XM_011517553.2:c.7699G>T
|
XP_011515855.1:p.Glu2567Ter
|
|
XM_011517554.3:c.7699G>T
|
XP_011515856.1:p.Glu2567Ter
|
|
XM_011517555.2:c.7696G>T
|
XP_011515857.1:p.Glu2566Ter
|
|
XM_017013612.1:c.7699G>T
|
XP_016869101.1:p.Glu2567Ter
|
|
XM_017013613.1:c.7606G>T
|
XP_016869102.1:p.Glu2536Ter
|
|
NM_017780.4:c.7609G>T
MANE Select
|
NP_060250.2:p.Glu2537Ter
|
|