ENST00000322344.8:c.1411C>A
MANE Select
|
ENSP00000323511.2:p.His471Asn
|
|
ENST00000636840.1:c.59+122C>A
|
|
|
ENST00000640501.1:c.17C>A
|
|
|
ENST00000322344.7:c.1411C>A
|
ENSP00000323511.2:p.His471Asn
|
|
ENST00000593946.5:c.*1338C>A
|
ENSP00000468896.1:n.*1338C>A
|
|
ENST00000594661.5:n.1912C>A
|
|
|
ENST00000595081.5:n.314C>A
|
|
|
ENST00000596014.5:c.1411C>A
|
ENSP00000472300.1:p.His471Asn
|
|
ENST00000597965.2:c.118C>A
|
ENSP00000471097.2:p.His40Asn
|
|
ENST00000599454.5:n.331C>A
|
|
|
ENST00000600573.5:c.1318C>A
|
ENSP00000469826.1:p.His440Asn
|
|
ENST00000600910.5:c.1301C>A
|
ENSP00000473137.1:p.Ser434Ter
|
|
ENST00000601816.3:n.483C>A
|
|
|
ENST00000625216.2:c.492C>A
|
ENSP00000486898.1:n.492C>A
|
|
ENST00000627232.2:c.1331C>A
|
ENSP00000486037.1:n.1331C>A
|
|
ENST00000631020.2:c.1303C>A
|
ENSP00000486707.1:p.His435Asn
|
|
NM_007254.3:c.1411C>A
|
NP_009185.2:p.His471Asn
|
|
NM_007254.4:c.1411C>A
MANE Select
|
NP_009185.2:p.His471Asn
|
|