ENST00000346342.8:c.309C>T
MANE Select
|
ENSP00000329546.4:p.Leu103=
|
|
ENST00000346342.7:c.309C>T
|
ENSP00000329546.3:p.Leu103=
|
|
ENST00000375581.3:c.375C>T
|
ENSP00000364731.3:p.Leu125=
|
|
ENST00000444337.1:c.*117C>T
|
ENSP00000387669.1:n.*117C>T
|
|
ENST00000473085.1:n.256C>T
|
|
|
ENST00000479674.1:n.642C>T
|
|
|
ENST00000541084.5:c.123C>T
|
ENSP00000442051.2:p.Leu41=
|
|
NM_000131.4:c.375C>T , LRG_554t1:c.375C>T
|
NP_000122.1:p.Leu125=
|
|
NM_001267554.1:c.123C>T
|
NP_001254483.1:p.Leu41=
|
|
NM_019616.3:c.309C>T , LRG_554t2:c.309C>T
|
NP_062562.1:p.Leu103=
|
|
NR_051961.1:n.396C>T
|
|
|
XM_006719963.2:c.309C>T
|
XP_006720026.1:p.Leu103=
|
|
XM_011537474.1:c.309C>T
|
XP_011535776.1:p.Leu103=
|
|
XM_011537475.1:c.123C>T
|
XP_011535777.1:p.Leu41=
|
|
XM_011537477.1:c.270C>T
|
XP_011535779.1:p.Leu90=
|
|
XM_006719963.3:c.354C>T
|
XP_006720026.2:p.Leu118=
|
|
XM_011537474.2:c.354C>T
|
XP_011535776.2:p.Leu118=
|
|
XM_011537475.2:c.168C>T
|
XP_011535777.2:p.Leu56=
|
|
NM_019616.4:c.309C>T
MANE Select
|
NP_062562.1:p.Leu103=
|
|
NR_051961.2:n.393C>T
|
|
|
NM_001267554.2:c.123C>T
|
NP_001254483.1:p.Leu41=
|
|