ENST00000695853.1:c.6588C>A
|
ENSP00000512218.1:p.Thr2196=
|
|
ENST00000423902.7:c.6588C>A
MANE Select
|
ENSP00000392028.1:p.Thr2196=
|
|
ENST00000423902.6:c.6588C>A
|
ENSP00000392028.1:p.Thr2196=
|
|
ENST00000524602.5:c.1717-8916C>A
|
ENSP00000437061.1:n.1717-8916C>A
|
|
NM_001316690.1:c.1717-8916C>A
|
NP_001303619.1:n.1717-8916C>A
|
|
NM_017780.3:c.6588C>A
|
NP_060250.2:p.Thr2196=
|
|
XM_011517553.1:c.6678C>A
|
XP_011515855.1:p.Thr2226=
|
|
XM_011517554.1:c.6678C>A
|
XP_011515856.1:p.Thr2226=
|
|
XM_011517555.1:c.6678C>A
|
XP_011515857.1:p.Thr2226=
|
|
XM_011517556.1:c.6678C>A
|
XP_011515858.1:p.Thr2226=
|
|
XM_011517557.1:c.4665C>A
|
XP_011515859.1:p.Thr1555=
|
|
XM_011517558.1:c.4215C>A
|
XP_011515860.1:p.Thr1405=
|
|
XM_011517559.1:c.3423C>A
|
XP_011515861.1:p.Thr1141=
|
|
XM_011517553.2:c.6678C>A
|
XP_011515855.1:p.Thr2226=
|
|
XM_011517554.3:c.6678C>A
|
XP_011515856.1:p.Thr2226=
|
|
XM_011517555.2:c.6678C>A
|
XP_011515857.1:p.Thr2226=
|
|
XM_017013612.1:c.6678C>A
|
XP_016869101.1:p.Thr2226=
|
|
XM_017013613.1:c.6588C>A
|
XP_016869102.1:p.Thr2196=
|
|
NM_017780.4:c.6588C>A
MANE Select
|
NP_060250.2:p.Thr2196=
|
|