|
ENST00000367698.4:c.837T>C
MANE Select
|
ENSP00000356671.3:p.Cys279=
|
|
|
ENST00000367698.3:c.837T>C
|
ENSP00000356671.3:p.Cys279=
|
|
|
ENST00000487183.1:n.488T>C
|
|
|
|
ENST00000617423.4:c.559+1996T>C
|
ENSP00000478688.1:n.559+1996T>C
|
|
|
NM_000488.3:c.837T>C , LRG_577t1:c.837T>C
|
NP_000479.1:p.Cys279=
|
|
|
XM_005245198.2:c.693T>C
|
XP_005245255.1:p.Cys231=
|
|
|
NM_001365052.1:c.693T>C
|
NP_001351981.1:p.Cys231=
|
|
|
NM_000488.4:c.837T>C
MANE Select
|
NP_000479.1:p.Cys279=
|
|
|
NM_001365052.2:c.693T>C
|
NP_001351981.1:p.Cys231=
|
|
|
NM_001386302.1:c.960T>C
|
NP_001373231.1:p.Cys320=
|
|
|
NM_001386303.1:c.918T>C
|
NP_001373232.1:p.Cys306=
|
|
|
NM_001386304.1:c.816T>C
|
NP_001373233.1:p.Cys272=
|
|
|
NM_001386305.1:c.780T>C
|
NP_001373234.1:p.Cys260=
|
|
|
NM_001386306.1:c.621T>C
|
NP_001373235.1:p.Cys207=
|
|
