ENST00000369486.8:c.2935del
MANE Select
|
ENSP00000358498.4:p.Arg979AlafsTer15
|
|
ENST00000318837.6:c.2995del
|
ENSP00000321184.6:p.Arg999AlafsTer15
|
|
ENST00000369483.5:c.2995del
|
ENSP00000358495.1:p.Arg999AlafsTer15
|
|
ENST00000369486.7:c.2935del
|
ENSP00000358498.3:p.Arg979AlafsTer15
|
|
NM_001007237.2:c.2935del
|
NP_001007238.1:p.Arg979AlafsTer15
|
|
NM_001542.3:c.2995del
|
NP_001533.2:p.Arg999AlafsTer15
|
|
XM_005270793.2:c.2995del
|
XP_005270850.1:p.Arg999AlafsTer15
|
|
XM_005270794.3:c.2950del
|
XP_005270851.1:p.Arg984AlafsTer15
|
|
XM_006710593.2:c.3010del
|
XP_006710656.1:p.Arg1004AlafsTer15
|
|
XM_011541315.1:c.2995del
|
XP_011539617.1:p.Arg999AlafsTer15
|
|
XM_011541316.1:c.1324del
|
XP_011539618.1:p.Arg442AlafsTer15
|
|
NM_001542.4:c.2995del
|
NP_001533.2:p.Arg999AlafsTer15
|
|
XM_005270794.4:c.2950del
|
XP_005270851.1:p.Arg984AlafsTer15
|
|
XM_006710593.3:c.3010del
|
XP_006710656.1:p.Arg1004AlafsTer15
|
|
XM_011541316.2:c.1324del
|
XP_011539618.1:p.Arg442AlafsTer15
|
|
NM_001007237.3:c.2935del
MANE Select
|
NP_001007238.1:p.Arg979AlafsTer15
|
|