ENST00000367698.4:c.1063T>G
MANE Select
|
ENSP00000356671.3:p.Phe355Val
|
|
ENST00000367698.3:c.1063T>G
|
ENSP00000356671.3:p.Phe355Val
|
|
ENST00000617423.4:c.560-2149T>G
|
ENSP00000478688.1:n.560-2149T>G
|
|
NM_000488.3:c.1063T>G , LRG_577t1:c.1063T>G
|
NP_000479.1:p.Phe355Val
|
|
XM_005245198.2:c.919T>G
|
XP_005245255.1:p.Phe307Val
|
|
NM_001365052.1:c.919T>G
|
NP_001351981.1:p.Phe307Val
|
|
NM_000488.4:c.1063T>G
MANE Select
|
NP_000479.1:p.Phe355Val
|
|
NM_001365052.2:c.919T>G
|
NP_001351981.1:p.Phe307Val
|
|
NM_001386302.1:c.1186T>G
|
NP_001373231.1:p.Phe396Val
|
|
NM_001386303.1:c.1144T>G
|
NP_001373232.1:p.Phe382Val
|
|
NM_001386304.1:c.1042T>G
|
NP_001373233.1:p.Phe348Val
|
|
NM_001386305.1:c.1006T>G
|
NP_001373234.1:p.Phe336Val
|
|
NM_001386306.1:c.847T>G
|
NP_001373235.1:p.Phe283Val
|
|