ENST00000311907.10:c.678G=
MANE Select
|
ENSP00000308541.5:p.Ala226=
|
|
ENST00000311907.9:c.678G=
|
ENSP00000308541.5:p.Ala226=
|
|
ENST00000442468.1:c.648G=
|
ENSP00000387413.1:p.Ala216=
|
|
ENST00000490274.1:n.458G=
|
|
|
ENST00000530231.5:c.678G=
|
ENSP00000433907.1:p.Ala226=
|
|
NM_000506.3:c.678G=
|
NP_000497.1:p.Ala226=
|
|
NM_000506.4:c.678G= , LRG_551t1:c.678G=
|
NP_000497.1:p.Ala226=
|
|
NM_001311257.1:c.630G=
|
NP_001298186.1:p.Ala210=
|
|
XR_428840.2:n.722G=
|
|
|
XR_428840.4:n.713G=
|
|
|
NM_000506.5:c.678G=
MANE Select
|
NP_000497.1:p.Ala226=
|
|
NM_001311257.2:c.630G=
|
NP_001298186.1:p.Ala210=
|
|