ENST00000695850.1:n.1346G>T
|
|
|
ENST00000695852.1:n.277G>T
|
|
|
ENST00000695853.1:c.*1229G>T
|
ENSP00000512218.1:n.*1229G>T
|
|
ENST00000423902.7:c.8170G>T
MANE Select
|
ENSP00000392028.1:p.Glu2724Ter
|
|
ENST00000423902.6:c.8170G>T
|
ENSP00000392028.1:p.Glu2724Ter
|
|
ENST00000524602.5:c.2023G>T
|
ENSP00000437061.1:p.Glu675Ter
|
|
ENST00000528280.1:n.216G>T
|
|
|
ENST00000532149.1:n.592G>T
|
|
|
ENST00000618450.1:n.4206G>T
|
|
|
NM_001316690.1:c.2023G>T
|
NP_001303619.1:p.Glu675Ter
|
|
NM_017780.3:c.8170G>T
|
NP_060250.2:p.Glu2724Ter
|
|
XM_011517553.1:c.8260G>T
|
XP_011515855.1:p.Glu2754Ter
|
|
XM_011517554.1:c.8260G>T
|
XP_011515856.1:p.Glu2754Ter
|
|
XM_011517555.1:c.8257G>T
|
XP_011515857.1:p.Glu2753Ter
|
|
XM_011517556.1:c.8038G>T
|
XP_011515858.1:p.Glu2680Ter
|
|
XM_011517557.1:c.6247G>T
|
XP_011515859.1:p.Glu2083Ter
|
|
XM_011517558.1:c.5797G>T
|
XP_011515860.1:p.Glu1933Ter
|
|
XM_011517559.1:c.5005G>T
|
XP_011515861.1:p.Glu1669Ter
|
|
XM_011517553.2:c.8260G>T
|
XP_011515855.1:p.Glu2754Ter
|
|
XM_011517554.3:c.8260G>T
|
XP_011515856.1:p.Glu2754Ter
|
|
XM_011517555.2:c.8257G>T
|
XP_011515857.1:p.Glu2753Ter
|
|
XM_017013612.1:c.8260G>T
|
XP_016869101.1:p.Glu2754Ter
|
|
XM_017013613.1:c.8167G>T
|
XP_016869102.1:p.Glu2723Ter
|
|
NM_017780.4:c.8170G>T
MANE Select
|
NP_060250.2:p.Glu2724Ter
|
|