ENST00000695850.1:n.1530C>A
|
|
|
ENST00000695852.1:n.461C>A
|
|
|
ENST00000695853.1:c.*1413C>A
|
ENSP00000512218.1:n.*1413C>A
|
|
ENST00000423902.7:c.8354C>A
MANE Select
|
ENSP00000392028.1:p.Ala2785Asp
|
|
ENST00000423902.6:c.8354C>A
|
ENSP00000392028.1:p.Ala2785Asp
|
|
ENST00000524602.5:c.2207C>A
|
ENSP00000437061.1:p.Ala736Asp
|
|
ENST00000528280.1:n.400C>A
|
|
|
NM_001316690.1:c.2207C>A
|
NP_001303619.1:p.Ala736Asp
|
|
NM_017780.3:c.8354C>A
|
NP_060250.2:p.Ala2785Asp
|
|
XM_011517553.1:c.8444C>A
|
XP_011515855.1:p.Ala2815Asp
|
|
XM_011517554.1:c.8444C>A
|
XP_011515856.1:p.Ala2815Asp
|
|
XM_011517555.1:c.8441C>A
|
XP_011515857.1:p.Ala2814Asp
|
|
XM_011517556.1:c.8222C>A
|
XP_011515858.1:p.Ala2741Asp
|
|
XM_011517557.1:c.6431C>A
|
XP_011515859.1:p.Ala2144Asp
|
|
XM_011517558.1:c.5981C>A
|
XP_011515860.1:p.Ala1994Asp
|
|
XM_011517559.1:c.5189C>A
|
XP_011515861.1:p.Ala1730Asp
|
|
XM_011517553.2:c.8444C>A
|
XP_011515855.1:p.Ala2815Asp
|
|
XM_011517554.3:c.8444C>A
|
XP_011515856.1:p.Ala2815Asp
|
|
XM_011517555.2:c.8441C>A
|
XP_011515857.1:p.Ala2814Asp
|
|
XM_017013612.1:c.8444C>A
|
XP_016869101.1:p.Ala2815Asp
|
|
XM_017013613.1:c.8351C>A
|
XP_016869102.1:p.Ala2784Asp
|
|
NM_017780.4:c.8354C>A
MANE Select
|
NP_060250.2:p.Ala2785Asp
|
|