ENST00000367698.4:c.1065C>T
MANE Select
|
ENSP00000356671.3:p.Phe355=
|
|
ENST00000367698.3:c.1065C>T
|
ENSP00000356671.3:p.Phe355=
|
|
ENST00000617423.4:c.560-2147C>T
|
ENSP00000478688.1:n.560-2147C>T
|
|
NM_000488.3:c.1065C>T , LRG_577t1:c.1065C>T
|
NP_000479.1:p.Phe355=
|
|
XM_005245198.2:c.921C>T
|
XP_005245255.1:p.Phe307=
|
|
NM_001365052.1:c.921C>T
|
NP_001351981.1:p.Phe307=
|
|
NM_000488.4:c.1065C>T
MANE Select
|
NP_000479.1:p.Phe355=
|
|
NM_001365052.2:c.921C>T
|
NP_001351981.1:p.Phe307=
|
|
NM_001386302.1:c.1188C>T
|
NP_001373231.1:p.Phe396=
|
|
NM_001386303.1:c.1146C>T
|
NP_001373232.1:p.Phe382=
|
|
NM_001386304.1:c.1044C>T
|
NP_001373233.1:p.Phe348=
|
|
NM_001386305.1:c.1008C>T
|
NP_001373234.1:p.Phe336=
|
|
NM_001386306.1:c.849C>T
|
NP_001373235.1:p.Phe283=
|
|