ENST00000346342.8:c.841A=
MANE Select
|
ENSP00000329546.4:p.Ile281=
|
|
ENST00000346342.7:c.841A=
|
ENSP00000329546.3:p.Ile281=
|
|
ENST00000375581.3:c.907A=
|
ENSP00000364731.3:p.Ile303=
|
|
ENST00000541084.5:c.655A=
|
ENSP00000442051.2:p.Ile219=
|
|
NM_000131.4:c.907A= , LRG_554t1:c.907A=
|
NP_000122.1:p.Ile303=
|
|
NM_001267554.1:c.655A=
|
NP_001254483.1:p.Ile219=
|
|
NM_019616.3:c.841A= , LRG_554t2:c.841A=
|
NP_062562.1:p.Ile281=
|
|
NR_051961.1:n.928A=
|
|
|
XM_006719963.2:c.700A=
|
XP_006720026.1:p.Ile234=
|
|
XM_011537474.1:c.949A=
|
XP_011535776.1:p.Ile317=
|
|
XM_011537475.1:c.763A=
|
XP_011535777.1:p.Ile255=
|
|
XM_011537476.1:c.601A=
|
XP_011535778.1:p.Ile201=
|
|
XM_011537477.1:c.910A=
|
XP_011535779.1:p.Ile304=
|
|
XM_006719963.3:c.745A=
|
XP_006720026.2:p.Ile249=
|
|
XM_011537474.2:c.994A=
|
XP_011535776.2:p.Ile332=
|
|
XM_011537475.2:c.808A=
|
XP_011535777.2:p.Ile270=
|
|
XM_011537476.2:c.601A=
|
XP_011535778.1:p.Ile201=
|
|
NM_019616.4:c.841A=
MANE Select
|
NP_062562.1:p.Ile281=
|
|
NR_051961.2:n.925A=
|
|
|
NM_001267554.2:c.655A=
|
NP_001254483.1:p.Ile219=
|
|