ENST00000322344.8:c.992G>C
MANE Select
|
ENSP00000323511.2:p.Trp331Ser
|
|
ENST00000322344.7:c.992G>C
|
ENSP00000323511.2:p.Trp331Ser
|
|
ENST00000593706.3:n.347G>C
|
|
|
ENST00000593946.5:c.*919G>C
|
ENSP00000468896.1:n.*919G>C
|
|
ENST00000594661.5:n.1493G>C
|
|
|
ENST00000596014.5:c.992G>C
|
ENSP00000472300.1:p.Trp331Ser
|
|
ENST00000600573.5:c.937-127G>C
|
ENSP00000469826.1:n.937-127G>C
|
|
ENST00000600910.5:c.992G>C
|
ENSP00000473137.1:p.Trp331Ser
|
|
ENST00000625216.2:c.170G>C
|
ENSP00000486898.1:p.Trp57Ser
|
|
ENST00000627232.2:c.912G>C
|
ENSP00000486037.1:n.912G>C
|
|
ENST00000627317.1:c.613G>C
|
|
|
ENST00000629179.1:n.763G>C
|
|
|
ENST00000631020.2:c.884G>C
|
ENSP00000486707.1:p.Trp295Ser
|
|
NM_007254.3:c.992G>C
|
NP_009185.2:p.Trp331Ser
|
|
NM_007254.4:c.992G>C
MANE Select
|
NP_009185.2:p.Trp331Ser
|
|