ENST00000346342.8:c.1150G>C
MANE Select
|
ENSP00000329546.4:p.Gly384Arg
|
|
ENST00000346342.7:c.1150G>C
|
ENSP00000329546.3:p.Gly384Arg
|
|
ENST00000375581.3:c.1216G>C
|
ENSP00000364731.3:p.Gly406Arg
|
|
ENST00000541084.5:c.964G>C
|
ENSP00000442051.2:p.Gly322Arg
|
|
NM_000131.4:c.1216G>C , LRG_554t1:c.1216G>C
|
NP_000122.1:p.Gly406Arg
|
|
NM_001267554.1:c.964G>C
|
NP_001254483.1:p.Gly322Arg
|
|
NM_019616.3:c.1150G>C , LRG_554t2:c.1150G>C
|
NP_062562.1:p.Gly384Arg
|
|
NR_051961.1:n.1237G>C
|
|
|
XM_006719963.2:c.1009G>C
|
XP_006720026.1:p.Gly337Arg
|
|
XM_011537474.1:c.1258G>C
|
XP_011535776.1:p.Gly420Arg
|
|
XM_011537475.1:c.1072G>C
|
XP_011535777.1:p.Gly358Arg
|
|
XM_011537476.1:c.910G>C
|
XP_011535778.1:p.Gly304Arg
|
|
XM_011537477.1:c.1219G>C
|
XP_011535779.1:p.Gly407Arg
|
|
XM_006719963.3:c.1054G>C
|
XP_006720026.2:p.Gly352Arg
|
|
XM_011537474.2:c.1303G>C
|
XP_011535776.2:p.Gly435Arg
|
|
XM_011537475.2:c.1117G>C
|
XP_011535777.2:p.Gly373Arg
|
|
XM_011537476.2:c.910G>C
|
XP_011535778.1:p.Gly304Arg
|
|
NM_019616.4:c.1150G>C
MANE Select
|
NP_062562.1:p.Gly384Arg
|
|
NR_051961.2:n.1234G>C
|
|
|
NM_001267554.2:c.964G>C
|
NP_001254483.1:p.Gly322Arg
|
|