ENST00000695850.1:n.1487G>T
|
|
|
ENST00000695852.1:n.418G>T
|
|
|
ENST00000695853.1:c.*1370G>T
|
ENSP00000512218.1:n.*1370G>T
|
|
ENST00000423902.7:c.8311G>T
MANE Select
|
ENSP00000392028.1:p.Gly2771Cys
|
|
ENST00000423902.6:c.8311G>T
|
ENSP00000392028.1:p.Gly2771Cys
|
|
ENST00000524602.5:c.2164G>T
|
ENSP00000437061.1:p.Gly722Cys
|
|
ENST00000528280.1:n.357G>T
|
|
|
NM_001316690.1:c.2164G>T
|
NP_001303619.1:p.Gly722Cys
|
|
NM_017780.3:c.8311G>T
|
NP_060250.2:p.Gly2771Cys
|
|
XM_011517553.1:c.8401G>T
|
XP_011515855.1:p.Gly2801Cys
|
|
XM_011517554.1:c.8401G>T
|
XP_011515856.1:p.Gly2801Cys
|
|
XM_011517555.1:c.8398G>T
|
XP_011515857.1:p.Gly2800Cys
|
|
XM_011517556.1:c.8179G>T
|
XP_011515858.1:p.Gly2727Cys
|
|
XM_011517557.1:c.6388G>T
|
XP_011515859.1:p.Gly2130Cys
|
|
XM_011517558.1:c.5938G>T
|
XP_011515860.1:p.Gly1980Cys
|
|
XM_011517559.1:c.5146G>T
|
XP_011515861.1:p.Gly1716Cys
|
|
XM_011517553.2:c.8401G>T
|
XP_011515855.1:p.Gly2801Cys
|
|
XM_011517554.3:c.8401G>T
|
XP_011515856.1:p.Gly2801Cys
|
|
XM_011517555.2:c.8398G>T
|
XP_011515857.1:p.Gly2800Cys
|
|
XM_017013612.1:c.8401G>T
|
XP_016869101.1:p.Gly2801Cys
|
|
XM_017013613.1:c.8308G>T
|
XP_016869102.1:p.Gly2770Cys
|
|
NM_017780.4:c.8311G>T
MANE Select
|
NP_060250.2:p.Gly2771Cys
|
|