ENST00000346342.8:c.1325C>G
MANE Select
|
ENSP00000329546.4:p.Pro442Arg
|
|
ENST00000346342.7:c.1325C>G
|
ENSP00000329546.3:p.Pro442Arg
|
|
ENST00000375581.3:c.1391C>G
|
ENSP00000364731.3:p.Pro464Arg
|
|
ENST00000541084.5:c.1139C>G
|
ENSP00000442051.2:p.Pro380Arg
|
|
NM_000131.4:c.1391C>G , LRG_554t1:c.1391C>G
|
NP_000122.1:p.Pro464Arg
|
|
NM_001267554.1:c.1139C>G
|
NP_001254483.1:p.Pro380Arg
|
|
NM_019616.3:c.1325C>G , LRG_554t2:c.1325C>G
|
NP_062562.1:p.Pro442Arg
|
|
NR_051961.1:n.1412C>G
|
|
|
XM_006719963.2:c.1184C>G
|
XP_006720026.1:p.Pro395Arg
|
|
XM_011537474.1:c.1433C>G
|
XP_011535776.1:p.Pro478Arg
|
|
XM_011537475.1:c.1247C>G
|
XP_011535777.1:p.Pro416Arg
|
|
XM_011537476.1:c.1085C>G
|
XP_011535778.1:p.Pro362Arg
|
|
XM_011537477.1:c.1394C>G
|
XP_011535779.1:p.Pro465Arg
|
|
XM_006719963.3:c.1229C>G
|
XP_006720026.2:p.Pro410Arg
|
|
XM_011537474.2:c.1478C>G
|
XP_011535776.2:p.Pro493Arg
|
|
XM_011537475.2:c.1292C>G
|
XP_011535777.2:p.Pro431Arg
|
|
XM_011537476.2:c.1085C>G
|
XP_011535778.1:p.Pro362Arg
|
|
NM_019616.4:c.1325C>G
MANE Select
|
NP_062562.1:p.Pro442Arg
|
|
NR_051961.2:n.1409C>G
|
|
|
NM_001267554.2:c.1139C>G
|
NP_001254483.1:p.Pro380Arg
|
|