ENST00000695850.1:n.1384C>A
|
|
|
ENST00000695852.1:n.315C>A
|
|
|
ENST00000695853.1:c.*1267C>A
|
ENSP00000512218.1:n.*1267C>A
|
|
ENST00000423902.7:c.8208C>A
MANE Select
|
ENSP00000392028.1:p.Ala2736=
|
|
ENST00000423902.6:c.8208C>A
|
ENSP00000392028.1:p.Ala2736=
|
|
ENST00000524602.5:c.2061C>A
|
ENSP00000437061.1:p.Ala687=
|
|
ENST00000528280.1:n.254C>A
|
|
|
NM_001316690.1:c.2061C>A
|
NP_001303619.1:p.Ala687=
|
|
NM_017780.3:c.8208C>A
|
NP_060250.2:p.Ala2736=
|
|
XM_011517553.1:c.8298C>A
|
XP_011515855.1:p.Ala2766=
|
|
XM_011517554.1:c.8298C>A
|
XP_011515856.1:p.Ala2766=
|
|
XM_011517555.1:c.8295C>A
|
XP_011515857.1:p.Ala2765=
|
|
XM_011517556.1:c.8076C>A
|
XP_011515858.1:p.Ala2692=
|
|
XM_011517557.1:c.6285C>A
|
XP_011515859.1:p.Ala2095=
|
|
XM_011517558.1:c.5835C>A
|
XP_011515860.1:p.Ala1945=
|
|
XM_011517559.1:c.5043C>A
|
XP_011515861.1:p.Ala1681=
|
|
XM_011517553.2:c.8298C>A
|
XP_011515855.1:p.Ala2766=
|
|
XM_011517554.3:c.8298C>A
|
XP_011515856.1:p.Ala2766=
|
|
XM_011517555.2:c.8295C>A
|
XP_011515857.1:p.Ala2765=
|
|
XM_017013612.1:c.8298C>A
|
XP_016869101.1:p.Ala2766=
|
|
XM_017013613.1:c.8205C>A
|
XP_016869102.1:p.Ala2735=
|
|
NM_017780.4:c.8208C>A
MANE Select
|
NP_060250.2:p.Ala2736=
|
|