ENST00000695850.1:n.1393A>G
|
|
|
ENST00000695852.1:n.324A>G
|
|
|
ENST00000695853.1:c.*1276A>G
|
ENSP00000512218.1:n.*1276A>G
|
|
ENST00000423902.7:c.8217A>G
MANE Select
|
ENSP00000392028.1:p.Ser2739=
|
|
ENST00000423902.6:c.8217A>G
|
ENSP00000392028.1:p.Ser2739=
|
|
ENST00000524602.5:c.2070A>G
|
ENSP00000437061.1:p.Ser690=
|
|
ENST00000528280.1:n.263A>G
|
|
|
NM_001316690.1:c.2070A>G
|
NP_001303619.1:p.Ser690=
|
|
NM_017780.3:c.8217A>G
|
NP_060250.2:p.Ser2739=
|
|
XM_011517553.1:c.8307A>G
|
XP_011515855.1:p.Ser2769=
|
|
XM_011517554.1:c.8307A>G
|
XP_011515856.1:p.Ser2769=
|
|
XM_011517555.1:c.8304A>G
|
XP_011515857.1:p.Ser2768=
|
|
XM_011517556.1:c.8085A>G
|
XP_011515858.1:p.Ser2695=
|
|
XM_011517557.1:c.6294A>G
|
XP_011515859.1:p.Ser2098=
|
|
XM_011517558.1:c.5844A>G
|
XP_011515860.1:p.Ser1948=
|
|
XM_011517559.1:c.5052A>G
|
XP_011515861.1:p.Ser1684=
|
|
XM_011517553.2:c.8307A>G
|
XP_011515855.1:p.Ser2769=
|
|
XM_011517554.3:c.8307A>G
|
XP_011515856.1:p.Ser2769=
|
|
XM_011517555.2:c.8304A>G
|
XP_011515857.1:p.Ser2768=
|
|
XM_017013612.1:c.8307A>G
|
XP_016869101.1:p.Ser2769=
|
|
XM_017013613.1:c.8214A>G
|
XP_016869102.1:p.Ser2738=
|
|
NM_017780.4:c.8217A>G
MANE Select
|
NP_060250.2:p.Ser2739=
|
|