ENST00000262648.8:c.19_28delinsGGCGCGGTCC
MANE Select
|
ENSP00000262648.3:p.Gly7=
|
|
ENST00000262648.7:c.19_28delinsGGCGCGGTCC
|
ENSP00000262648.3:p.Gly7=
|
|
ENST00000619786.1:c.19_28delinsGGCGCGGTCC
|
ENSP00000478734.1:p.Gly7=
|
|
NM_000216.2:c.19_28delinsGGCGCGGTCC
|
NP_000207.2:p.Gly7=
|
|
XM_005274501.3:c.19_28delinsGGCGCGGTCC
|
XP_005274558.1:p.Gly7=
|
|
NM_000216.3:c.19_28delinsGGCGCGGTCC
|
NP_000207.2:p.Gly7=
|
|
XM_005274501.4:c.19_28delinsGGCGCGGTCC
|
XP_005274558.1:p.Gly7=
|
|
NM_000216.4:c.19_28delinsGGCGCGGTCC
MANE Select
|
NP_000207.2:p.Gly7=
|
|