ENST00000346342.8:c.763G=
MANE Select
|
ENSP00000329546.4:p.Asp255=
|
|
ENST00000346342.7:c.763G=
|
ENSP00000329546.3:p.Asp255=
|
|
ENST00000375581.3:c.829G=
|
ENSP00000364731.3:p.Asp277=
|
|
ENST00000541084.5:c.577G=
|
ENSP00000442051.2:p.Asp193=
|
|
NM_000131.4:c.829G= , LRG_554t1:c.829G=
|
NP_000122.1:p.Asp277=
|
|
NM_001267554.1:c.577G=
|
NP_001254483.1:p.Asp193=
|
|
NM_019616.3:c.763G= , LRG_554t2:c.763G=
|
NP_062562.1:p.Asp255=
|
|
NR_051961.1:n.850G=
|
|
|
XM_006719963.2:c.622G=
|
XP_006720026.1:p.Asp208=
|
|
XM_011537474.1:c.871G=
|
XP_011535776.1:p.Asp291=
|
|
XM_011537475.1:c.685G=
|
XP_011535777.1:p.Asp229=
|
|
XM_011537476.1:c.523G=
|
XP_011535778.1:p.Asp175=
|
|
XM_011537477.1:c.832G=
|
XP_011535779.1:p.Asp278=
|
|
XM_006719963.3:c.667G=
|
XP_006720026.2:p.Asp223=
|
|
XM_011537474.2:c.916G=
|
XP_011535776.2:p.Asp306=
|
|
XM_011537475.2:c.730G=
|
XP_011535777.2:p.Asp244=
|
|
XM_011537476.2:c.523G=
|
XP_011535778.1:p.Asp175=
|
|
NM_019616.4:c.763G=
MANE Select
|
NP_062562.1:p.Asp255=
|
|
NR_051961.2:n.847G=
|
|
|
NM_001267554.2:c.577G=
|
NP_001254483.1:p.Asp193=
|
|