ENST00000346342.8:c.1286T>G
MANE Select
|
ENSP00000329546.4:p.Met429Arg
|
|
ENST00000346342.7:c.1286T>G
|
ENSP00000329546.3:p.Met429Arg
|
|
ENST00000375581.3:c.1352T>G
|
ENSP00000364731.3:p.Met451Arg
|
|
ENST00000541084.5:c.1100T>G
|
ENSP00000442051.2:p.Met367Arg
|
|
NM_000131.4:c.1352T>G , LRG_554t1:c.1352T>G
|
NP_000122.1:p.Met451Arg
|
|
NM_001267554.1:c.1100T>G
|
NP_001254483.1:p.Met367Arg
|
|
NM_019616.3:c.1286T>G , LRG_554t2:c.1286T>G
|
NP_062562.1:p.Met429Arg
|
|
NR_051961.1:n.1373T>G
|
|
|
XM_006719963.2:c.1145T>G
|
XP_006720026.1:p.Met382Arg
|
|
XM_011537474.1:c.1394T>G
|
XP_011535776.1:p.Met465Arg
|
|
XM_011537475.1:c.1208T>G
|
XP_011535777.1:p.Met403Arg
|
|
XM_011537476.1:c.1046T>G
|
XP_011535778.1:p.Met349Arg
|
|
XM_011537477.1:c.1355T>G
|
XP_011535779.1:p.Met452Arg
|
|
XM_006719963.3:c.1190T>G
|
XP_006720026.2:p.Met397Arg
|
|
XM_011537474.2:c.1439T>G
|
XP_011535776.2:p.Met480Arg
|
|
XM_011537475.2:c.1253T>G
|
XP_011535777.2:p.Met418Arg
|
|
XM_011537476.2:c.1046T>G
|
XP_011535778.1:p.Met349Arg
|
|
NM_019616.4:c.1286T>G
MANE Select
|
NP_062562.1:p.Met429Arg
|
|
NR_051961.2:n.1370T>G
|
|
|
NM_001267554.2:c.1100T>G
|
NP_001254483.1:p.Met367Arg
|
|