ENST00000367698.4:c.875A>G
MANE Select
|
ENSP00000356671.3:p.Tyr292Cys
|
|
ENST00000367698.3:c.875A>G
|
ENSP00000356671.3:p.Tyr292Cys
|
|
ENST00000487183.1:n.526A>G
|
|
|
ENST00000617423.4:c.559+2034A>G
|
ENSP00000478688.1:n.559+2034A>G
|
|
NM_000488.3:c.875A>G , LRG_577t1:c.875A>G
|
NP_000479.1:p.Tyr292Cys
|
|
XM_005245198.2:c.731A>G
|
XP_005245255.1:p.Tyr244Cys
|
|
NM_001365052.1:c.731A>G
|
NP_001351981.1:p.Tyr244Cys
|
|
NM_000488.4:c.875A>G
MANE Select
|
NP_000479.1:p.Tyr292Cys
|
|
NM_001365052.2:c.731A>G
|
NP_001351981.1:p.Tyr244Cys
|
|
NM_001386302.1:c.998A>G
|
NP_001373231.1:p.Tyr333Cys
|
|
NM_001386303.1:c.956A>G
|
NP_001373232.1:p.Tyr319Cys
|
|
NM_001386304.1:c.854A>G
|
NP_001373233.1:p.Tyr285Cys
|
|
NM_001386305.1:c.818A>G
|
NP_001373234.1:p.Tyr273Cys
|
|
NM_001386306.1:c.659A>G
|
NP_001373235.1:p.Tyr220Cys
|
|