ENST00000221515.6:c.302C=
MANE Select
|
ENSP00000221515.1:p.Ala101=
|
|
ENST00000221515.5:c.302C=
|
ENSP00000221515.1:p.Ala101=
|
|
ENST00000381324.2:c.224C=
|
ENSP00000370725.2:p.Ala75=
|
|
ENST00000629642.1:c.224C=
|
ENSP00000485998.1:p.Ala75=
|
|
NM_001193374.1:c.302C=
|
NP_001180303.1:p.Ala101=
|
|
NM_020415.3:c.302C=
|
NP_065148.1:p.Ala101=
|
|
NM_020415.4:c.302C=
MANE Select
|
NP_065148.1:p.Ala101=
|
|
NM_001193374.2:c.302C=
|
NP_001180303.1:p.Ala101=
|
|
NM_001385725.1:c.302C=
|
NP_001372654.1:p.Ala101=
|
|
NM_001385726.1:c.344C=
|
NP_001372655.1:p.Ala115=
|
|
NM_001385727.1:c.224C=
|
NP_001372656.1:p.Ala75=
|
|