NM_001166.5:c.1517C>T
MANE Select
|
NP_001157.1:p.Ala506Val
|
ENST00000227758.7:c.1517C>T
MANE Select
|
ENSP00000227758.2:p.Ala506Val
|
NM_001166.4:c.1517C>T
|
NP_001157.1:p.Ala506Val
|
NM_001256163.1:c.1517C>T
|
NP_001243092.1:p.Ala506Val
|
NM_001256166.1:c.1370C>T
|
NP_001243095.1:p.Ala457Val
|
NM_001256166.2:c.1370C>T
|
NP_001243095.1:p.Ala457Val
|
ENST00000227758.6:c.1517C>T
|
ENSP00000227758.2:p.Ala506Val
|
ENST00000527910.5:n.3246C>T
|
|
ENST00000530675.5:c.1370C>T
|
ENSP00000431723.1:p.Ala457Val
|
ENST00000531259.5:c.122C>T
|
ENSP00000436741.1:p.Ala41Val
|
ENST00000532672.5:c.1454C>T
|
ENSP00000434979.1:p.Ala485Val
|
ENST00000533742.5:c.503C>T
|
ENSP00000433851.1:p.Ala168Val
|
ENST00000613397.4:c.1517C>T
|
ENSP00000477613.1:p.Ala506Val
|
ENST00000621637.1:c.1517C>T
|
ENSP00000484838.1:p.Ala506Val
|