ENST00000346342.8:c.816C>T
MANE Select
|
ENSP00000329546.4:p.Tyr272=
|
|
ENST00000346342.7:c.816C>T
|
ENSP00000329546.3:p.Tyr272=
|
|
ENST00000375581.3:c.882C>T
|
ENSP00000364731.3:p.Tyr294=
|
|
ENST00000541084.5:c.630C>T
|
ENSP00000442051.2:p.Tyr210=
|
|
NM_000131.4:c.882C>T , LRG_554t1:c.882C>T
|
NP_000122.1:p.Tyr294=
|
|
NM_001267554.1:c.630C>T
|
NP_001254483.1:p.Tyr210=
|
|
NM_019616.3:c.816C>T , LRG_554t2:c.816C>T
|
NP_062562.1:p.Tyr272=
|
|
NR_051961.1:n.903C>T
|
|
|
XM_006719963.2:c.675C>T
|
XP_006720026.1:p.Tyr225=
|
|
XM_011537474.1:c.924C>T
|
XP_011535776.1:p.Tyr308=
|
|
XM_011537475.1:c.738C>T
|
XP_011535777.1:p.Tyr246=
|
|
XM_011537476.1:c.576C>T
|
XP_011535778.1:p.Tyr192=
|
|
XM_011537477.1:c.885C>T
|
XP_011535779.1:p.Tyr295=
|
|
XM_006719963.3:c.720C>T
|
XP_006720026.2:p.Tyr240=
|
|
XM_011537474.2:c.969C>T
|
XP_011535776.2:p.Tyr323=
|
|
XM_011537475.2:c.783C>T
|
XP_011535777.2:p.Tyr261=
|
|
XM_011537476.2:c.576C>T
|
XP_011535778.1:p.Tyr192=
|
|
NM_019616.4:c.816C>T
MANE Select
|
NP_062562.1:p.Tyr272=
|
|
NR_051961.2:n.900C>T
|
|
|
NM_001267554.2:c.630C>T
|
NP_001254483.1:p.Tyr210=
|
|