NM_000455.5:c.1249dup
MANE Select
|
NP_000446.1:p.Ala417GlyfsTer?
|
ENST00000326873.12:c.1249dup
MANE Select
|
ENSP00000324856.6:p.Ala417GlyfsTer?
|
NM_000455.4:c.1249dup , LRG_319t1:c.1249dup
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NP_000446.1:p.Ala417GlyfsTer?
|
ENST00000326873.11:c.1249dup
|
ENSP00000324856.6:p.Ala417GlyfsTer?
|
ENST00000585465.2:n.2982dup
|
|
ENST00000585465.3:c.*2850dup
|
ENSP00000490268.2:n.*2850dup
|
ENST00000585748.3:c.877dup
|
ENSP00000477641.2:p.Ala293GlyfsTer?
|
ENST00000585851.2:c.1075dup
|
ENSP00000467912.2:p.Ala359GlyfsTer?
|
ENST00000586243.5:c.1248dup
|
ENSP00000467240.2:p.Pro417AlafsTer?
|
ENST00000589152.5:n.1947dup
|
|
XM_005259617.1:c.1244dup
|
XP_005259674.1:p.Leu416ProfsTer?
|
XM_005259617.3:c.1244dup
|
XP_005259674.1:p.Leu416ProfsTer?
|
XM_011528209.1:c.1022dup
|
XP_011526511.1:p.Leu342ProfsTer?
|
XM_011528209.2:c.1022dup
|
XP_011526511.1:p.Leu342ProfsTer?
|
XR_001753738.2:n.2055dup
|
|
XR_001753740.2:n.2025dup
|
|