ENST00000329956.11:c.1526G>A
MANE Select
|
ENSP00000329943.6:p.Gly509Asp
|
|
ENST00000329956.10:c.1526G>A
|
ENSP00000329943.6:p.Gly509Asp
|
|
ENST00000435835.3:c.1132-3311G>A
|
ENSP00000411122.3:n.1132-3311G>A
|
|
ENST00000563189.5:c.1163G>A
|
ENSP00000455103.1:p.Gly388Asp
|
|
ENST00000565019.6:c.1072-37G>A
|
|
|
ENST00000567723.5:c.*852G>A
|
ENSP00000455799.1:n.*852G>A
|
|
ENST00000567823.5:c.*21G>A
|
ENSP00000456164.1:n.*21G>A
|
|
ENST00000568010.5:c.*266G>A
|
ENSP00000455018.1:n.*266G>A
|
|
NM_001161575.1:c.1163G>A
|
NP_001155047.1:p.Gly388Asp
|
|
NM_018296.5:c.1526G>A
|
NP_060766.5:p.Gly509Asp
|
|
XM_005256025.2:c.1526G>A
|
XP_005256082.1:p.Gly509Asp
|
|
XM_005256026.2:c.1085G>A
|
XP_005256083.1:p.Gly362Asp
|
|
XM_005256027.2:c.1526G>A
|
XP_005256084.1:p.Gly509Asp
|
|
XM_005256028.1:c.1022G>A
|
XP_005256085.1:p.Gly341Asp
|
|
XM_011523199.1:c.1526G>A
|
XP_011521501.1:p.Gly509Asp
|
|
XM_011523200.1:c.1526G>A
|
XP_011521502.1:p.Gly509Asp
|
|
XM_011523201.1:c.1022G>A
|
XP_011521503.1:p.Gly341Asp
|
|
XM_011523202.1:c.1019G>A
|
XP_011521504.1:p.Gly340Asp
|
|
XM_011523203.1:c.908G>A
|
XP_011521505.1:p.Gly303Asp
|
|
XM_011523204.1:c.800G>A
|
XP_011521506.1:p.Gly267Asp
|
|
XM_011523205.1:c.800G>A
|
XP_011521507.1:p.Gly267Asp
|
|
XR_243416.2:n.1545G>A
|
|
|
XR_429723.1:n.1534G>A
|
|
|
XM_011523202.2:c.1019G>A
|
XP_011521504.1:p.Gly340Asp
|
|
XM_017023400.2:c.1526G>A
|
XP_016878889.1:p.Gly509Asp
|
|
XM_017023401.1:c.775G>A
|
XP_016878890.1:p.Val259Ile
|
|
XM_017023402.1:c.598G>A
|
XP_016878891.1:p.Val200Ile
|
|
XM_024450338.1:c.800G>A
|
XP_024306106.1:p.Gly267Asp
|
|
NM_018296.6:c.1526G>A
MANE Select
|
NP_060766.5:p.Gly509Asp
|
|
NM_001161575.2:c.1163G>A
|
NP_001155047.1:p.Gly388Asp
|
|