ENST00000322344.8:c.1392A>C
MANE Select
|
ENSP00000323511.2:p.Arg464=
|
|
ENST00000636840.1:c.59+103A>C
|
|
|
ENST00000322344.7:c.1392A>C
|
ENSP00000323511.2:p.Arg464=
|
|
ENST00000593946.5:c.*1319A>C
|
ENSP00000468896.1:n.*1319A>C
|
|
ENST00000594661.5:n.1893A>C
|
|
|
ENST00000595081.5:n.295A>C
|
|
|
ENST00000596014.5:c.1392A>C
|
ENSP00000472300.1:p.Arg464=
|
|
ENST00000597965.2:c.99A>C
|
ENSP00000471097.2:p.Arg33=
|
|
ENST00000599454.5:n.312A>C
|
|
|
ENST00000600573.5:c.1299A>C
|
ENSP00000469826.1:p.Arg433=
|
|
ENST00000600910.5:c.1282A>C
|
ENSP00000473137.1:p.Arg428=
|
|
ENST00000601816.3:n.464A>C
|
|
|
ENST00000625216.2:c.473A>C
|
ENSP00000486898.1:n.473A>C
|
|
ENST00000627232.2:c.1312A>C
|
ENSP00000486037.1:n.1312A>C
|
|
ENST00000631020.2:c.1284A>C
|
ENSP00000486707.1:p.Arg428=
|
|
NM_007254.3:c.1392A>C
|
NP_009185.2:p.Arg464=
|
|
NM_007254.4:c.1392A>C
MANE Select
|
NP_009185.2:p.Arg464=
|
|