ENST00000367698.4:c.421G>T
MANE Select
|
ENSP00000356671.3:p.Asp141Tyr
|
|
ENST00000367698.3:c.421G>T
|
ENSP00000356671.3:p.Asp141Tyr
|
|
ENST00000487183.1:n.126G>T
|
|
|
ENST00000494024.1:n.647G>T
|
|
|
ENST00000617423.4:c.421G>T
|
ENSP00000478688.1:p.Asp141Tyr
|
|
NM_000488.3:c.421G>T , LRG_577t1:c.421G>T
|
NP_000479.1:p.Asp141Tyr
|
|
XM_005245198.2:c.277G>T
|
XP_005245255.1:p.Asp93Tyr
|
|
NM_001365052.1:c.277G>T
|
NP_001351981.1:p.Asp93Tyr
|
|
NM_000488.4:c.421G>T
MANE Select
|
NP_000479.1:p.Asp141Tyr
|
|
NM_001365052.2:c.277G>T
|
NP_001351981.1:p.Asp93Tyr
|
|
NM_001386302.1:c.421G>T
|
NP_001373231.1:p.Asp141Tyr
|
|
NM_001386303.1:c.502G>T
|
NP_001373232.1:p.Asp168Tyr
|
|
NM_001386304.1:c.421G>T
|
NP_001373233.1:p.Asp141Tyr
|
|
NM_001386305.1:c.421G>T
|
NP_001373234.1:p.Asp141Tyr
|
|
NM_001386306.1:c.409-1111G>T
|
NP_001373235.1:n.409-1111G>T
|
|