ENST00000695850.1:n.876C>G
|
|
|
ENST00000695851.1:n.80C>G
|
|
|
ENST00000695853.1:c.*759C>G
|
ENSP00000512218.1:n.*759C>G
|
|
ENST00000423902.7:c.7700C>G
MANE Select
|
ENSP00000392028.1:p.Thr2567Arg
|
|
ENST00000423902.6:c.7700C>G
|
ENSP00000392028.1:p.Thr2567Arg
|
|
ENST00000524602.5:c.1717-1234C>G
|
ENSP00000437061.1:n.1717-1234C>G
|
|
ENST00000531695.1:n.124C>G
|
|
|
ENST00000618450.1:n.92C>G
|
|
|
NM_001316690.1:c.1717-1234C>G
|
NP_001303619.1:n.1717-1234C>G
|
|
NM_017780.3:c.7700C>G
|
NP_060250.2:p.Thr2567Arg
|
|
XM_011517553.1:c.7790C>G
|
XP_011515855.1:p.Thr2597Arg
|
|
XM_011517554.1:c.7790C>G
|
XP_011515856.1:p.Thr2597Arg
|
|
XM_011517555.1:c.7787C>G
|
XP_011515857.1:p.Thr2596Arg
|
|
XM_011517556.1:c.7699-1201C>G
|
XP_011515858.1:n.7699-1201C>G
|
|
XM_011517557.1:c.5777C>G
|
XP_011515859.1:p.Thr1926Arg
|
|
XM_011517558.1:c.5327C>G
|
XP_011515860.1:p.Thr1776Arg
|
|
XM_011517559.1:c.4535C>G
|
XP_011515861.1:p.Thr1512Arg
|
|
XM_011517553.2:c.7790C>G
|
XP_011515855.1:p.Thr2597Arg
|
|
XM_011517554.3:c.7790C>G
|
XP_011515856.1:p.Thr2597Arg
|
|
XM_011517555.2:c.7787C>G
|
XP_011515857.1:p.Thr2596Arg
|
|
XM_017013612.1:c.7790C>G
|
XP_016869101.1:p.Thr2597Arg
|
|
XM_017013613.1:c.7697C>G
|
XP_016869102.1:p.Thr2566Arg
|
|
NM_017780.4:c.7700C>G
MANE Select
|
NP_060250.2:p.Thr2567Arg
|
|