ENST00000456935.7:c.1125C=
MANE Select
|
ENSP00000395473.2:p.Asp375=
|
|
ENST00000221363.8:c.1122C=
|
ENSP00000221363.4:p.Asp374=
|
|
ENST00000456935.6:c.1125C=
|
ENSP00000395473.2:p.Asp375=
|
|
ENST00000465830.1:n.289C=
|
|
|
ENST00000466794.5:n.1024C=
|
|
|
ENST00000495617.1:n.280+402C=
|
|
|
NM_000528.3:c.1125C=
|
NP_000519.2:p.Asp375=
|
|
NM_001173498.1:c.1122C=
|
NP_001166969.1:p.Asp374=
|
|
XM_005259913.1:c.1128C=
|
XP_005259970.1:p.Asp376=
|
|
XM_011528017.1:c.24C=
|
XP_011526319.1:p.Asp8=
|
|
XM_005259913.2:c.1128C=
|
XP_005259970.1:p.Asp376=
|
|
XM_024451518.1:c.24C=
|
XP_024307286.1:p.Asp8=
|
|
NM_000528.4:c.1125C=
MANE Select
|
NP_000519.2:p.Asp375=
|
|
NM_001173498.2:c.1122C=
|
NP_001166969.1:p.Asp374=
|
|