ENST00000367698.4:c.815A>G
MANE Select
|
ENSP00000356671.3:p.Tyr272Cys
|
|
ENST00000367698.3:c.815A>G
|
ENSP00000356671.3:p.Tyr272Cys
|
|
ENST00000487183.1:n.466A>G
|
|
|
ENST00000617423.4:c.559+1974A>G
|
ENSP00000478688.1:n.559+1974A>G
|
|
NM_000488.3:c.815A>G , LRG_577t1:c.815A>G
|
NP_000479.1:p.Tyr272Cys
|
|
XM_005245198.2:c.671A>G
|
XP_005245255.1:p.Tyr224Cys
|
|
NM_001365052.1:c.671A>G
|
NP_001351981.1:p.Tyr224Cys
|
|
NM_000488.4:c.815A>G
MANE Select
|
NP_000479.1:p.Tyr272Cys
|
|
NM_001365052.2:c.671A>G
|
NP_001351981.1:p.Tyr224Cys
|
|
NM_001386302.1:c.938A>G
|
NP_001373231.1:p.Tyr313Cys
|
|
NM_001386303.1:c.896A>G
|
NP_001373232.1:p.Tyr299Cys
|
|
NM_001386304.1:c.794A>G
|
NP_001373233.1:p.Tyr265Cys
|
|
NM_001386305.1:c.763-5A>G
|
NP_001373234.1:n.763-5A>G
|
|
NM_001386306.1:c.599A>G
|
NP_001373235.1:p.Tyr200Cys
|
|