ENST00000695850.1:n.910T>G
|
|
|
ENST00000695851.1:n.114T>G
|
|
|
ENST00000695853.1:c.*793T>G
|
ENSP00000512218.1:n.*793T>G
|
|
ENST00000423902.7:c.7734T>G
MANE Select
|
ENSP00000392028.1:p.Thr2578=
|
|
ENST00000423902.6:c.7734T>G
|
ENSP00000392028.1:p.Thr2578=
|
|
ENST00000524602.5:c.1717-1200T>G
|
ENSP00000437061.1:n.1717-1200T>G
|
|
ENST00000531695.1:n.158T>G
|
|
|
ENST00000618450.1:n.126T>G
|
|
|
NM_001316690.1:c.1717-1200T>G
|
NP_001303619.1:n.1717-1200T>G
|
|
NM_017780.3:c.7734T>G
|
NP_060250.2:p.Thr2578=
|
|
XM_011517553.1:c.7824T>G
|
XP_011515855.1:p.Thr2608=
|
|
XM_011517554.1:c.7824T>G
|
XP_011515856.1:p.Thr2608=
|
|
XM_011517555.1:c.7821T>G
|
XP_011515857.1:p.Thr2607=
|
|
XM_011517556.1:c.7699-1167T>G
|
XP_011515858.1:n.7699-1167T>G
|
|
XM_011517557.1:c.5811T>G
|
XP_011515859.1:p.Thr1937=
|
|
XM_011517558.1:c.5361T>G
|
XP_011515860.1:p.Thr1787=
|
|
XM_011517559.1:c.4569T>G
|
XP_011515861.1:p.Thr1523=
|
|
XM_011517553.2:c.7824T>G
|
XP_011515855.1:p.Thr2608=
|
|
XM_011517554.3:c.7824T>G
|
XP_011515856.1:p.Thr2608=
|
|
XM_011517555.2:c.7821T>G
|
XP_011515857.1:p.Thr2607=
|
|
XM_017013612.1:c.7824T>G
|
XP_016869101.1:p.Thr2608=
|
|
XM_017013613.1:c.7731T>G
|
XP_016869102.1:p.Thr2577=
|
|
NM_017780.4:c.7734T>G
MANE Select
|
NP_060250.2:p.Thr2578=
|
|