ENST00000367698.4:c.835T>G
MANE Select
|
ENSP00000356671.3:p.Cys279Gly
|
|
ENST00000367698.3:c.835T>G
|
ENSP00000356671.3:p.Cys279Gly
|
|
ENST00000487183.1:n.486T>G
|
|
|
ENST00000617423.4:c.559+1994T>G
|
ENSP00000478688.1:n.559+1994T>G
|
|
NM_000488.3:c.835T>G , LRG_577t1:c.835T>G
|
NP_000479.1:p.Cys279Gly
|
|
XM_005245198.2:c.691T>G
|
XP_005245255.1:p.Cys231Gly
|
|
NM_001365052.1:c.691T>G
|
NP_001351981.1:p.Cys231Gly
|
|
NM_000488.4:c.835T>G
MANE Select
|
NP_000479.1:p.Cys279Gly
|
|
NM_001365052.2:c.691T>G
|
NP_001351981.1:p.Cys231Gly
|
|
NM_001386302.1:c.958T>G
|
NP_001373231.1:p.Cys320Gly
|
|
NM_001386303.1:c.916T>G
|
NP_001373232.1:p.Cys306Gly
|
|
NM_001386304.1:c.814T>G
|
NP_001373233.1:p.Cys272Gly
|
|
NM_001386305.1:c.778T>G
|
NP_001373234.1:p.Cys260Gly
|
|
NM_001386306.1:c.619T>G
|
NP_001373235.1:p.Cys207Gly
|
|