ENST00000585465.3:c.*2813C=
|
ENSP00000490268.2:n.*2813C=
|
|
ENST00000585748.3:c.840C=
|
ENSP00000477641.2:p.Ser280=
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|
ENST00000585851.2:c.1038C=
|
ENSP00000467912.2:p.Ser346=
|
|
ENST00000326873.12:c.1212C=
MANE Select
|
ENSP00000324856.6:p.Ser404=
|
|
ENST00000326873.11:c.1212C=
|
ENSP00000324856.6:p.Ser404=
|
|
ENST00000585465.2:n.2945C=
|
|
|
ENST00000586243.5:c.1212C=
|
ENSP00000467240.2:p.Ser404=
|
|
ENST00000589152.5:n.1910C=
|
|
|
NM_000455.4:c.1212C= , LRG_319t1:c.1212C=
|
NP_000446.1:p.Ser404=
|
|
XM_005259617.1:c.1207C=
|
XP_005259674.1:p.Gln403=
|
|
XM_011528209.1:c.985C=
|
XP_011526511.1:p.Gln329=
|
|
XM_005259617.3:c.1207C=
|
XP_005259674.1:p.Gln403=
|
|
XM_011528209.2:c.985C=
|
XP_011526511.1:p.Gln329=
|
|
XR_001753738.2:n.2018C=
|
|
|
XR_001753740.2:n.1988C=
|
|
|
NM_000455.5:c.1212C=
MANE Select
|
NP_000446.1:p.Ser404=
|
|