ENST00000695850.1:n.1374C>A
|
|
|
ENST00000695852.1:n.305C>A
|
|
|
ENST00000695853.1:c.*1257C>A
|
ENSP00000512218.1:n.*1257C>A
|
|
ENST00000423902.7:c.8198C>A
MANE Select
|
ENSP00000392028.1:p.Ala2733Asp
|
|
ENST00000423902.6:c.8198C>A
|
ENSP00000392028.1:p.Ala2733Asp
|
|
ENST00000524602.5:c.2051C>A
|
ENSP00000437061.1:p.Ala684Asp
|
|
ENST00000528280.1:n.244C>A
|
|
|
NM_001316690.1:c.2051C>A
|
NP_001303619.1:p.Ala684Asp
|
|
NM_017780.3:c.8198C>A
|
NP_060250.2:p.Ala2733Asp
|
|
XM_011517553.1:c.8288C>A
|
XP_011515855.1:p.Ala2763Asp
|
|
XM_011517554.1:c.8288C>A
|
XP_011515856.1:p.Ala2763Asp
|
|
XM_011517555.1:c.8285C>A
|
XP_011515857.1:p.Ala2762Asp
|
|
XM_011517556.1:c.8066C>A
|
XP_011515858.1:p.Ala2689Asp
|
|
XM_011517557.1:c.6275C>A
|
XP_011515859.1:p.Ala2092Asp
|
|
XM_011517558.1:c.5825C>A
|
XP_011515860.1:p.Ala1942Asp
|
|
XM_011517559.1:c.5033C>A
|
XP_011515861.1:p.Ala1678Asp
|
|
XM_011517553.2:c.8288C>A
|
XP_011515855.1:p.Ala2763Asp
|
|
XM_011517554.3:c.8288C>A
|
XP_011515856.1:p.Ala2763Asp
|
|
XM_011517555.2:c.8285C>A
|
XP_011515857.1:p.Ala2762Asp
|
|
XM_017013612.1:c.8288C>A
|
XP_016869101.1:p.Ala2763Asp
|
|
XM_017013613.1:c.8195C>A
|
XP_016869102.1:p.Ala2732Asp
|
|
NM_017780.4:c.8198C>A
MANE Select
|
NP_060250.2:p.Ala2733Asp
|
|