ENST00000695850.1:n.829C>A
|
|
|
ENST00000695851.1:n.33C>A
|
|
|
ENST00000695853.1:c.*712C>A
|
ENSP00000512218.1:n.*712C>A
|
|
ENST00000423902.7:c.7653C>A
MANE Select
|
ENSP00000392028.1:p.Thr2551=
|
|
ENST00000423902.6:c.7653C>A
|
ENSP00000392028.1:p.Thr2551=
|
|
ENST00000524602.5:c.1717-1281C>A
|
ENSP00000437061.1:n.1717-1281C>A
|
|
ENST00000531695.1:n.77C>A
|
|
|
ENST00000618450.1:n.45C>A
|
|
|
NM_001316690.1:c.1717-1281C>A
|
NP_001303619.1:n.1717-1281C>A
|
|
NM_017780.3:c.7653C>A
|
NP_060250.2:p.Thr2551=
|
|
XM_011517553.1:c.7743C>A
|
XP_011515855.1:p.Thr2581=
|
|
XM_011517554.1:c.7743C>A
|
XP_011515856.1:p.Thr2581=
|
|
XM_011517555.1:c.7740C>A
|
XP_011515857.1:p.Thr2580=
|
|
XM_011517556.1:c.7699-1248C>A
|
XP_011515858.1:n.7699-1248C>A
|
|
XM_011517557.1:c.5730C>A
|
XP_011515859.1:p.Thr1910=
|
|
XM_011517558.1:c.5280C>A
|
XP_011515860.1:p.Thr1760=
|
|
XM_011517559.1:c.4488C>A
|
XP_011515861.1:p.Thr1496=
|
|
XM_011517553.2:c.7743C>A
|
XP_011515855.1:p.Thr2581=
|
|
XM_011517554.3:c.7743C>A
|
XP_011515856.1:p.Thr2581=
|
|
XM_011517555.2:c.7740C>A
|
XP_011515857.1:p.Thr2580=
|
|
XM_017013612.1:c.7743C>A
|
XP_016869101.1:p.Thr2581=
|
|
XM_017013613.1:c.7650C>A
|
XP_016869102.1:p.Thr2550=
|
|
NM_017780.4:c.7653C>A
MANE Select
|
NP_060250.2:p.Thr2551=
|
|