|
ENST00000367698.4:c.825T>C
MANE Select
|
ENSP00000356671.3:p.Asp275=
|
|
|
ENST00000367698.3:c.825T>C
|
ENSP00000356671.3:p.Asp275=
|
|
|
ENST00000487183.1:n.476T>C
|
|
|
|
ENST00000617423.4:c.559+1984T>C
|
ENSP00000478688.1:n.559+1984T>C
|
|
|
NM_000488.3:c.825T>C , LRG_577t1:c.825T>C
|
NP_000479.1:p.Asp275=
|
|
|
XM_005245198.2:c.681T>C
|
XP_005245255.1:p.Asp227=
|
|
|
NM_001365052.1:c.681T>C
|
NP_001351981.1:p.Asp227=
|
|
|
NM_000488.4:c.825T>C
MANE Select
|
NP_000479.1:p.Asp275=
|
|
|
NM_001365052.2:c.681T>C
|
NP_001351981.1:p.Asp227=
|
|
|
NM_001386302.1:c.948T>C
|
NP_001373231.1:p.Asp316=
|
|
|
NM_001386303.1:c.906T>C
|
NP_001373232.1:p.Asp302=
|
|
|
NM_001386304.1:c.804T>C
|
NP_001373233.1:p.Asp268=
|
|
|
NM_001386305.1:c.768T>C
|
NP_001373234.1:p.Asp256=
|
|
|
NM_001386306.1:c.609T>C
|
NP_001373235.1:p.Asp203=
|
|
