ENST00000695850.1:n.877A>T
|
|
|
ENST00000695851.1:n.81A>T
|
|
|
ENST00000695853.1:c.*760A>T
|
ENSP00000512218.1:n.*760A>T
|
|
ENST00000423902.7:c.7701A>T
MANE Select
|
ENSP00000392028.1:p.Thr2567=
|
|
ENST00000423902.6:c.7701A>T
|
ENSP00000392028.1:p.Thr2567=
|
|
ENST00000524602.5:c.1717-1233A>T
|
ENSP00000437061.1:n.1717-1233A>T
|
|
ENST00000531695.1:n.125A>T
|
|
|
ENST00000618450.1:n.93A>T
|
|
|
NM_001316690.1:c.1717-1233A>T
|
NP_001303619.1:n.1717-1233A>T
|
|
NM_017780.3:c.7701A>T
|
NP_060250.2:p.Thr2567=
|
|
XM_011517553.1:c.7791A>T
|
XP_011515855.1:p.Thr2597=
|
|
XM_011517554.1:c.7791A>T
|
XP_011515856.1:p.Thr2597=
|
|
XM_011517555.1:c.7788A>T
|
XP_011515857.1:p.Thr2596=
|
|
XM_011517556.1:c.7699-1200A>T
|
XP_011515858.1:n.7699-1200A>T
|
|
XM_011517557.1:c.5778A>T
|
XP_011515859.1:p.Thr1926=
|
|
XM_011517558.1:c.5328A>T
|
XP_011515860.1:p.Thr1776=
|
|
XM_011517559.1:c.4536A>T
|
XP_011515861.1:p.Thr1512=
|
|
XM_011517553.2:c.7791A>T
|
XP_011515855.1:p.Thr2597=
|
|
XM_011517554.3:c.7791A>T
|
XP_011515856.1:p.Thr2597=
|
|
XM_011517555.2:c.7788A>T
|
XP_011515857.1:p.Thr2596=
|
|
XM_017013612.1:c.7791A>T
|
XP_016869101.1:p.Thr2597=
|
|
XM_017013613.1:c.7698A>T
|
XP_016869102.1:p.Thr2566=
|
|
NM_017780.4:c.7701A>T
MANE Select
|
NP_060250.2:p.Thr2567=
|
|