ENST00000695850.1:n.819A>C
|
|
|
ENST00000695851.1:n.23A>C
|
|
|
ENST00000695853.1:c.*702A>C
|
ENSP00000512218.1:n.*702A>C
|
|
ENST00000423902.7:c.7643A>C
MANE Select
|
ENSP00000392028.1:p.Asp2548Ala
|
|
ENST00000423902.6:c.7643A>C
|
ENSP00000392028.1:p.Asp2548Ala
|
|
ENST00000524602.5:c.1717-1291A>C
|
ENSP00000437061.1:n.1717-1291A>C
|
|
ENST00000531695.1:n.67A>C
|
|
|
ENST00000618450.1:n.35A>C
|
|
|
NM_001316690.1:c.1717-1291A>C
|
NP_001303619.1:n.1717-1291A>C
|
|
NM_017780.3:c.7643A>C
|
NP_060250.2:p.Asp2548Ala
|
|
XM_011517553.1:c.7733A>C
|
XP_011515855.1:p.Asp2578Ala
|
|
XM_011517554.1:c.7733A>C
|
XP_011515856.1:p.Asp2578Ala
|
|
XM_011517555.1:c.7730A>C
|
XP_011515857.1:p.Asp2577Ala
|
|
XM_011517556.1:c.7699-1258A>C
|
XP_011515858.1:n.7699-1258A>C
|
|
XM_011517557.1:c.5720A>C
|
XP_011515859.1:p.Asp1907Ala
|
|
XM_011517558.1:c.5270A>C
|
XP_011515860.1:p.Asp1757Ala
|
|
XM_011517559.1:c.4478A>C
|
XP_011515861.1:p.Asp1493Ala
|
|
XM_011517553.2:c.7733A>C
|
XP_011515855.1:p.Asp2578Ala
|
|
XM_011517554.3:c.7733A>C
|
XP_011515856.1:p.Asp2578Ala
|
|
XM_011517555.2:c.7730A>C
|
XP_011515857.1:p.Asp2577Ala
|
|
XM_017013612.1:c.7733A>C
|
XP_016869101.1:p.Asp2578Ala
|
|
XM_017013613.1:c.7640A>C
|
XP_016869102.1:p.Asp2547Ala
|
|
NM_017780.4:c.7643A>C
MANE Select
|
NP_060250.2:p.Asp2548Ala
|
|