ENST00000651692.1:c.429_431delinsCTT
|
ENSP00000498849.1:p.Asp143=
|
|
ENST00000652676.1:n.459-386_459-384delinsCTT
|
|
|
ENST00000347364.7:c.429_431delinsCTT
MANE Select
|
ENSP00000246062.4:p.Asp143=
|
|
ENST00000399054.6:c.429_431delinsCTT
|
ENSP00000382008.2:p.Asp143=
|
|
NM_018848.3:c.429_431delinsCTT
|
NP_061336.1:p.Asp143=
|
|
NM_170784.2:c.429_431delinsCTT
|
NP_740754.1:p.Asp143=
|
|
NR_072977.1:n.364-4283_364-4281delinsCTT
|
|
|
NR_072977.2:n.347-4283_347-4281delinsCTT
|
|
|
NM_170784.3:c.429_431delinsCTT
MANE Select
|
NP_740754.1:p.Asp143=
|
|