ENST00000322344.8:c.1447A>T
MANE Select
|
ENSP00000323511.2:p.Arg483Trp
|
|
ENST00000636840.1:c.59+158A>T
|
|
|
ENST00000640501.1:c.53A>T
|
|
|
ENST00000322344.7:c.1447A>T
|
ENSP00000323511.2:p.Arg483Trp
|
|
ENST00000593946.5:c.*1374A>T
|
ENSP00000468896.1:n.*1374A>T
|
|
ENST00000594661.5:n.1948A>T
|
|
|
ENST00000595081.5:n.350A>T
|
|
|
ENST00000596014.5:c.1447A>T
|
ENSP00000472300.1:p.Arg483Trp
|
|
ENST00000597965.2:c.154A>T
|
ENSP00000471097.2:p.Arg52Trp
|
|
ENST00000599454.5:n.367A>T
|
|
|
ENST00000600573.5:c.1354A>T
|
ENSP00000469826.1:p.Arg452Trp
|
|
ENST00000600910.5:c.1337A>T
|
ENSP00000473137.1:p.Gln446Leu
|
|
ENST00000601816.3:n.519A>T
|
|
|
ENST00000625216.2:c.528A>T
|
ENSP00000486898.1:n.528A>T
|
|
ENST00000627232.2:c.1367A>T
|
ENSP00000486037.1:n.1367A>T
|
|
ENST00000631020.2:c.1339A>T
|
ENSP00000486707.1:p.Arg447Trp
|
|
NM_007254.3:c.1447A>T
|
NP_009185.2:p.Arg483Trp
|
|
NM_007254.4:c.1447A>T
MANE Select
|
NP_009185.2:p.Arg483Trp
|
|