ENST00000329956.11:c.1513G>T
MANE Select
|
ENSP00000329943.6:p.Gly505Cys
|
|
ENST00000329956.10:c.1513G>T
|
ENSP00000329943.6:p.Gly505Cys
|
|
ENST00000435835.3:c.1132-3324G>T
|
ENSP00000411122.3:n.1132-3324G>T
|
|
ENST00000563189.5:c.1150G>T
|
ENSP00000455103.1:p.Gly384Cys
|
|
ENST00000565019.6:c.1072-50G>T
|
|
|
ENST00000567723.5:c.*839G>T
|
ENSP00000455799.1:n.*839G>T
|
|
ENST00000567823.5:c.*8G>T
|
ENSP00000456164.1:n.*8G>T
|
|
ENST00000568010.5:c.*253G>T
|
ENSP00000455018.1:n.*253G>T
|
|
NM_001161575.1:c.1150G>T
|
NP_001155047.1:p.Gly384Cys
|
|
NM_018296.5:c.1513G>T
|
NP_060766.5:p.Gly505Cys
|
|
XM_005256025.2:c.1513G>T
|
XP_005256082.1:p.Gly505Cys
|
|
XM_005256026.2:c.1072G>T
|
XP_005256083.1:p.Gly358Cys
|
|
XM_005256027.2:c.1513G>T
|
XP_005256084.1:p.Gly505Cys
|
|
XM_005256028.1:c.1009G>T
|
XP_005256085.1:p.Gly337Cys
|
|
XM_011523199.1:c.1513G>T
|
XP_011521501.1:p.Gly505Cys
|
|
XM_011523200.1:c.1513G>T
|
XP_011521502.1:p.Gly505Cys
|
|
XM_011523201.1:c.1009G>T
|
XP_011521503.1:p.Gly337Cys
|
|
XM_011523202.1:c.1006G>T
|
XP_011521504.1:p.Gly336Cys
|
|
XM_011523203.1:c.895G>T
|
XP_011521505.1:p.Gly299Cys
|
|
XM_011523204.1:c.787G>T
|
XP_011521506.1:p.Gly263Cys
|
|
XM_011523205.1:c.787G>T
|
XP_011521507.1:p.Gly263Cys
|
|
XR_243416.2:n.1532G>T
|
|
|
XR_429723.1:n.1521G>T
|
|
|
XM_011523202.2:c.1006G>T
|
XP_011521504.1:p.Gly336Cys
|
|
XM_017023400.2:c.1513G>T
|
XP_016878889.1:p.Gly505Cys
|
|
XM_017023401.1:c.762G>T
|
XP_016878890.1:p.Trp254Cys
|
|
XM_017023402.1:c.585G>T
|
XP_016878891.1:p.Trp195Cys
|
|
XM_024450338.1:c.787G>T
|
XP_024306106.1:p.Gly263Cys
|
|
NM_018296.6:c.1513G>T
MANE Select
|
NP_060766.5:p.Gly505Cys
|
|
NM_001161575.2:c.1150G>T
|
NP_001155047.1:p.Gly384Cys
|
|