ENST00000346342.8:c.844G=
MANE Select
|
ENSP00000329546.4:p.Ala282=
|
|
ENST00000346342.7:c.844G=
|
ENSP00000329546.3:p.Ala282=
|
|
ENST00000375581.3:c.910G=
|
ENSP00000364731.3:p.Ala304=
|
|
ENST00000541084.5:c.658G=
|
ENSP00000442051.2:p.Ala220=
|
|
NM_000131.4:c.910G= , LRG_554t1:c.910G=
|
NP_000122.1:p.Ala304=
|
|
NM_001267554.1:c.658G=
|
NP_001254483.1:p.Ala220=
|
|
NM_019616.3:c.844G= , LRG_554t2:c.844G=
|
NP_062562.1:p.Ala282=
|
|
NR_051961.1:n.931G=
|
|
|
XM_006719963.2:c.703G=
|
XP_006720026.1:p.Ala235=
|
|
XM_011537474.1:c.952G=
|
XP_011535776.1:p.Ala318=
|
|
XM_011537475.1:c.766G=
|
XP_011535777.1:p.Ala256=
|
|
XM_011537476.1:c.604G=
|
XP_011535778.1:p.Ala202=
|
|
XM_011537477.1:c.913G=
|
XP_011535779.1:p.Ala305=
|
|
XM_006719963.3:c.748G=
|
XP_006720026.2:p.Ala250=
|
|
XM_011537474.2:c.997G=
|
XP_011535776.2:p.Ala333=
|
|
XM_011537475.2:c.811G=
|
XP_011535777.2:p.Ala271=
|
|
XM_011537476.2:c.604G=
|
XP_011535778.1:p.Ala202=
|
|
NM_019616.4:c.844G=
MANE Select
|
NP_062562.1:p.Ala282=
|
|
NR_051961.2:n.928G=
|
|
|
NM_001267554.2:c.658G=
|
NP_001254483.1:p.Ala220=
|
|