ENST00000261978.9:c.4800T>A
MANE Select
|
ENSP00000261978.4:p.Arg1600=
|
|
ENST00000261978.8:c.4800T>A
|
ENSP00000261978.4:p.Arg1600=
|
|
ENST00000553939.5:c.4800T>A
|
ENSP00000452110.1:p.Arg1600=
|
|
ENST00000556690.5:c.4668T>A
|
ENSP00000451477.1:p.Arg1556=
|
|
NM_000428.2:c.4800T>A
|
NP_000419.1:p.Arg1600=
|
|
XM_011536765.1:c.4419T>A
|
XP_011535067.1:p.Arg1473=
|
|
XM_011536766.1:c.4341T>A
|
XP_011535068.1:p.Arg1447=
|
|
XM_011536767.1:c.4317T>A
|
XP_011535069.1:p.Arg1439=
|
|
XM_011536765.2:c.4419T>A
|
XP_011535067.1:p.Arg1473=
|
|
NM_000428.3:c.4800T>A
MANE Select
|
NP_000419.1:p.Arg1600=
|
|