ENST00000695850.1:n.1383C>A
|
|
|
ENST00000695852.1:n.314C>A
|
|
|
ENST00000695853.1:c.*1266C>A
|
ENSP00000512218.1:n.*1266C>A
|
|
ENST00000423902.7:c.8207C>A
MANE Select
|
ENSP00000392028.1:p.Ala2736Asp
|
|
ENST00000423902.6:c.8207C>A
|
ENSP00000392028.1:p.Ala2736Asp
|
|
ENST00000524602.5:c.2060C>A
|
ENSP00000437061.1:p.Ala687Asp
|
|
ENST00000528280.1:n.253C>A
|
|
|
NM_001316690.1:c.2060C>A
|
NP_001303619.1:p.Ala687Asp
|
|
NM_017780.3:c.8207C>A
|
NP_060250.2:p.Ala2736Asp
|
|
XM_011517553.1:c.8297C>A
|
XP_011515855.1:p.Ala2766Asp
|
|
XM_011517554.1:c.8297C>A
|
XP_011515856.1:p.Ala2766Asp
|
|
XM_011517555.1:c.8294C>A
|
XP_011515857.1:p.Ala2765Asp
|
|
XM_011517556.1:c.8075C>A
|
XP_011515858.1:p.Ala2692Asp
|
|
XM_011517557.1:c.6284C>A
|
XP_011515859.1:p.Ala2095Asp
|
|
XM_011517558.1:c.5834C>A
|
XP_011515860.1:p.Ala1945Asp
|
|
XM_011517559.1:c.5042C>A
|
XP_011515861.1:p.Ala1681Asp
|
|
XM_011517553.2:c.8297C>A
|
XP_011515855.1:p.Ala2766Asp
|
|
XM_011517554.3:c.8297C>A
|
XP_011515856.1:p.Ala2766Asp
|
|
XM_011517555.2:c.8294C>A
|
XP_011515857.1:p.Ala2765Asp
|
|
XM_017013612.1:c.8297C>A
|
XP_016869101.1:p.Ala2766Asp
|
|
XM_017013613.1:c.8204C>A
|
XP_016869102.1:p.Ala2735Asp
|
|
NM_017780.4:c.8207C>A
MANE Select
|
NP_060250.2:p.Ala2736Asp
|
|