ENST00000346342.8:c.799A=
MANE Select
|
ENSP00000329546.4:p.Ile267=
|
|
ENST00000346342.7:c.799A=
|
ENSP00000329546.3:p.Ile267=
|
|
ENST00000375581.3:c.865A=
|
ENSP00000364731.3:p.Ile289=
|
|
ENST00000541084.5:c.613A=
|
ENSP00000442051.2:p.Ile205=
|
|
NM_000131.4:c.865A= , LRG_554t1:c.865A=
|
NP_000122.1:p.Ile289=
|
|
NM_001267554.1:c.613A=
|
NP_001254483.1:p.Ile205=
|
|
NM_019616.3:c.799A= , LRG_554t2:c.799A=
|
NP_062562.1:p.Ile267=
|
|
NR_051961.1:n.886A=
|
|
|
XM_006719963.2:c.658A=
|
XP_006720026.1:p.Ile220=
|
|
XM_011537474.1:c.907A=
|
XP_011535776.1:p.Ile303=
|
|
XM_011537475.1:c.721A=
|
XP_011535777.1:p.Ile241=
|
|
XM_011537476.1:c.559A=
|
XP_011535778.1:p.Ile187=
|
|
XM_011537477.1:c.868A=
|
XP_011535779.1:p.Ile290=
|
|
XM_006719963.3:c.703A=
|
XP_006720026.2:p.Ile235=
|
|
XM_011537474.2:c.952A=
|
XP_011535776.2:p.Ile318=
|
|
XM_011537475.2:c.766A=
|
XP_011535777.2:p.Ile256=
|
|
XM_011537476.2:c.559A=
|
XP_011535778.1:p.Ile187=
|
|
NM_019616.4:c.799A=
MANE Select
|
NP_062562.1:p.Ile267=
|
|
NR_051961.2:n.883A=
|
|
|
NM_001267554.2:c.613A=
|
NP_001254483.1:p.Ile205=
|
|