ENST00000695850.1:n.1006+193A>T
|
|
|
ENST00000695851.1:n.210+193A>T
|
|
|
ENST00000695853.1:c.*889+193A>T
|
ENSP00000512218.1:n.*889+193A>T
|
|
ENST00000423902.7:c.7830+193A>T
MANE Select
|
ENSP00000392028.1:n.7830+193A>T
|
|
ENST00000423902.6:c.7830+193A>T
|
ENSP00000392028.1:n.7830+193A>T
|
|
ENST00000524602.5:c.1717-911A>T
|
ENSP00000437061.1:n.1717-911A>T
|
|
ENST00000531695.1:n.447A>T
|
|
|
ENST00000618450.1:n.415A>T
|
|
|
NM_001316690.1:c.1717-911A>T
|
NP_001303619.1:n.1717-911A>T
|
|
NM_017780.3:c.7830+193A>T
|
NP_060250.2:n.7830+193A>T
|
|
XM_011517553.1:c.7920+193A>T
|
XP_011515855.1:n.7920+193A>T
|
|
XM_011517554.1:c.7920+193A>T
|
XP_011515856.1:n.7920+193A>T
|
|
XM_011517555.1:c.7917+193A>T
|
XP_011515857.1:n.7917+193A>T
|
|
XM_011517556.1:c.7699-878A>T
|
XP_011515858.1:n.7699-878A>T
|
|
XM_011517557.1:c.5907+193A>T
|
XP_011515859.1:n.5907+193A>T
|
|
XM_011517558.1:c.5457+193A>T
|
XP_011515860.1:n.5457+193A>T
|
|
XM_011517559.1:c.4665+193A>T
|
XP_011515861.1:n.4665+193A>T
|
|
XM_011517553.2:c.7920+193A>T
|
XP_011515855.1:n.7920+193A>T
|
|
XM_011517554.3:c.7920+193A>T
|
XP_011515856.1:n.7920+193A>T
|
|
XM_011517555.2:c.7917+193A>T
|
XP_011515857.1:n.7917+193A>T
|
|
XM_017013612.1:c.7920+193A>T
|
XP_016869101.1:n.7920+193A>T
|
|
XM_017013613.1:c.7827+193A>T
|
XP_016869102.1:n.7827+193A>T
|
|
NM_017780.4:c.7830+193A>T
MANE Select
|
NP_060250.2:n.7830+193A>T
|
|