ENST00000346342.8:c.804C>T
MANE Select
|
ENSP00000329546.4:p.Ile268=
|
|
ENST00000346342.7:c.804C>T
|
ENSP00000329546.3:p.Ile268=
|
|
ENST00000375581.3:c.870C>T
|
ENSP00000364731.3:p.Ile290=
|
|
ENST00000541084.5:c.618C>T
|
ENSP00000442051.2:p.Ile206=
|
|
NM_000131.4:c.870C>T , LRG_554t1:c.870C>T
|
NP_000122.1:p.Ile290=
|
|
NM_001267554.1:c.618C>T
|
NP_001254483.1:p.Ile206=
|
|
NM_019616.3:c.804C>T , LRG_554t2:c.804C>T
|
NP_062562.1:p.Ile268=
|
|
NR_051961.1:n.891C>T
|
|
|
XM_006719963.2:c.663C>T
|
XP_006720026.1:p.Ile221=
|
|
XM_011537474.1:c.912C>T
|
XP_011535776.1:p.Ile304=
|
|
XM_011537475.1:c.726C>T
|
XP_011535777.1:p.Ile242=
|
|
XM_011537476.1:c.564C>T
|
XP_011535778.1:p.Ile188=
|
|
XM_011537477.1:c.873C>T
|
XP_011535779.1:p.Ile291=
|
|
XM_006719963.3:c.708C>T
|
XP_006720026.2:p.Ile236=
|
|
XM_011537474.2:c.957C>T
|
XP_011535776.2:p.Ile319=
|
|
XM_011537475.2:c.771C>T
|
XP_011535777.2:p.Ile257=
|
|
XM_011537476.2:c.564C>T
|
XP_011535778.1:p.Ile188=
|
|
NM_019616.4:c.804C>T
MANE Select
|
NP_062562.1:p.Ile268=
|
|
NR_051961.2:n.888C>T
|
|
|
NM_001267554.2:c.618C>T
|
NP_001254483.1:p.Ile206=
|
|