ENST00000695850.1:n.1328G>A
|
|
|
ENST00000695852.1:n.259G>A
|
|
|
ENST00000695853.1:c.*1211G>A
|
ENSP00000512218.1:n.*1211G>A
|
|
ENST00000423902.7:c.8152G>A
MANE Select
|
ENSP00000392028.1:p.Gly2718Arg
|
|
ENST00000423902.6:c.8152G>A
|
ENSP00000392028.1:p.Gly2718Arg
|
|
ENST00000524602.5:c.2005G>A
|
ENSP00000437061.1:p.Gly669Arg
|
|
ENST00000528280.1:n.198G>A
|
|
|
ENST00000532149.1:n.574G>A
|
|
|
ENST00000618450.1:n.4188G>A
|
|
|
NM_001316690.1:c.2005G>A
|
NP_001303619.1:p.Gly669Arg
|
|
NM_017780.3:c.8152G>A
|
NP_060250.2:p.Gly2718Arg
|
|
XM_011517553.1:c.8242G>A
|
XP_011515855.1:p.Gly2748Arg
|
|
XM_011517554.1:c.8242G>A
|
XP_011515856.1:p.Gly2748Arg
|
|
XM_011517555.1:c.8239G>A
|
XP_011515857.1:p.Gly2747Arg
|
|
XM_011517556.1:c.8020G>A
|
XP_011515858.1:p.Gly2674Arg
|
|
XM_011517557.1:c.6229G>A
|
XP_011515859.1:p.Gly2077Arg
|
|
XM_011517558.1:c.5779G>A
|
XP_011515860.1:p.Gly1927Arg
|
|
XM_011517559.1:c.4987G>A
|
XP_011515861.1:p.Gly1663Arg
|
|
XM_011517553.2:c.8242G>A
|
XP_011515855.1:p.Gly2748Arg
|
|
XM_011517554.3:c.8242G>A
|
XP_011515856.1:p.Gly2748Arg
|
|
XM_011517555.2:c.8239G>A
|
XP_011515857.1:p.Gly2747Arg
|
|
XM_017013612.1:c.8242G>A
|
XP_016869101.1:p.Gly2748Arg
|
|
XM_017013613.1:c.8149G>A
|
XP_016869102.1:p.Gly2717Arg
|
|
NM_017780.4:c.8152G>A
MANE Select
|
NP_060250.2:p.Gly2718Arg
|
|