ENST00000346342.8:c.1318C>G
MANE Select
|
ENSP00000329546.4:p.Arg440Gly
|
|
ENST00000346342.7:c.1318C>G
|
ENSP00000329546.3:p.Arg440Gly
|
|
ENST00000375581.3:c.1384C>G
|
ENSP00000364731.3:p.Arg462Gly
|
|
ENST00000541084.5:c.1132C>G
|
ENSP00000442051.2:p.Arg378Gly
|
|
NM_000131.4:c.1384C>G , LRG_554t1:c.1384C>G
|
NP_000122.1:p.Arg462Gly
|
|
NM_001267554.1:c.1132C>G
|
NP_001254483.1:p.Arg378Gly
|
|
NM_019616.3:c.1318C>G , LRG_554t2:c.1318C>G
|
NP_062562.1:p.Arg440Gly
|
|
NR_051961.1:n.1405C>G
|
|
|
XM_006719963.2:c.1177C>G
|
XP_006720026.1:p.Arg393Gly
|
|
XM_011537474.1:c.1426C>G
|
XP_011535776.1:p.Arg476Gly
|
|
XM_011537475.1:c.1240C>G
|
XP_011535777.1:p.Arg414Gly
|
|
XM_011537476.1:c.1078C>G
|
XP_011535778.1:p.Arg360Gly
|
|
XM_011537477.1:c.1387C>G
|
XP_011535779.1:p.Arg463Gly
|
|
XM_006719963.3:c.1222C>G
|
XP_006720026.2:p.Arg408Gly
|
|
XM_011537474.2:c.1471C>G
|
XP_011535776.2:p.Arg491Gly
|
|
XM_011537475.2:c.1285C>G
|
XP_011535777.2:p.Arg429Gly
|
|
XM_011537476.2:c.1078C>G
|
XP_011535778.1:p.Arg360Gly
|
|
NM_019616.4:c.1318C>G
MANE Select
|
NP_062562.1:p.Arg440Gly
|
|
NR_051961.2:n.1402C>G
|
|
|
NM_001267554.2:c.1132C>G
|
NP_001254483.1:p.Arg378Gly
|
|