ENST00000346342.8:c.1316T=
MANE Select
|
ENSP00000329546.4:p.Leu439=
|
|
ENST00000346342.7:c.1316T=
|
ENSP00000329546.3:p.Leu439=
|
|
ENST00000375581.3:c.1382T=
|
ENSP00000364731.3:p.Leu461=
|
|
ENST00000541084.5:c.1130T=
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ENSP00000442051.2:p.Leu377=
|
|
NM_000131.4:c.1382T= , LRG_554t1:c.1382T=
|
NP_000122.1:p.Leu461=
|
|
NM_001267554.1:c.1130T=
|
NP_001254483.1:p.Leu377=
|
|
NM_019616.3:c.1316T= , LRG_554t2:c.1316T=
|
NP_062562.1:p.Leu439=
|
|
NR_051961.1:n.1403T=
|
|
|
XM_006719963.2:c.1175T=
|
XP_006720026.1:p.Leu392=
|
|
XM_011537474.1:c.1424T=
|
XP_011535776.1:p.Leu475=
|
|
XM_011537475.1:c.1238T=
|
XP_011535777.1:p.Leu413=
|
|
XM_011537476.1:c.1076T=
|
XP_011535778.1:p.Leu359=
|
|
XM_011537477.1:c.1385T=
|
XP_011535779.1:p.Leu462=
|
|
XM_006719963.3:c.1220T=
|
XP_006720026.2:p.Leu407=
|
|
XM_011537474.2:c.1469T=
|
XP_011535776.2:p.Leu490=
|
|
XM_011537475.2:c.1283T=
|
XP_011535777.2:p.Leu428=
|
|
XM_011537476.2:c.1076T=
|
XP_011535778.1:p.Leu359=
|
|
NM_019616.4:c.1316T=
MANE Select
|
NP_062562.1:p.Leu439=
|
|
NR_051961.2:n.1400T=
|
|
|
NM_001267554.2:c.1130T=
|
NP_001254483.1:p.Leu377=
|
|