ENST00000367698.4:c.853T>G
MANE Select
|
ENSP00000356671.3:p.Tyr285Asp
|
|
ENST00000367698.3:c.853T>G
|
ENSP00000356671.3:p.Tyr285Asp
|
|
ENST00000487183.1:n.504T>G
|
|
|
ENST00000617423.4:c.559+2012T>G
|
ENSP00000478688.1:n.559+2012T>G
|
|
NM_000488.3:c.853T>G , LRG_577t1:c.853T>G
|
NP_000479.1:p.Tyr285Asp
|
|
XM_005245198.2:c.709T>G
|
XP_005245255.1:p.Tyr237Asp
|
|
NM_001365052.1:c.709T>G
|
NP_001351981.1:p.Tyr237Asp
|
|
NM_000488.4:c.853T>G
MANE Select
|
NP_000479.1:p.Tyr285Asp
|
|
NM_001365052.2:c.709T>G
|
NP_001351981.1:p.Tyr237Asp
|
|
NM_001386302.1:c.976T>G
|
NP_001373231.1:p.Tyr326Asp
|
|
NM_001386303.1:c.934T>G
|
NP_001373232.1:p.Tyr312Asp
|
|
NM_001386304.1:c.832T>G
|
NP_001373233.1:p.Tyr278Asp
|
|
NM_001386305.1:c.796T>G
|
NP_001373234.1:p.Tyr266Asp
|
|
NM_001386306.1:c.637T>G
|
NP_001373235.1:p.Tyr213Asp
|
|