ENST00000322344.8:c.983T>C
MANE Select
|
ENSP00000323511.2:p.Phe328Ser
|
|
ENST00000322344.7:c.983T>C
|
ENSP00000323511.2:p.Phe328Ser
|
|
ENST00000593706.3:n.338T>C
|
|
|
ENST00000593946.5:c.*910T>C
|
ENSP00000468896.1:n.*910T>C
|
|
ENST00000594661.5:n.1484T>C
|
|
|
ENST00000596014.5:c.983T>C
|
ENSP00000472300.1:p.Phe328Ser
|
|
ENST00000600573.5:c.936+121T>C
|
ENSP00000469826.1:n.936+121T>C
|
|
ENST00000600910.5:c.983T>C
|
ENSP00000473137.1:p.Phe328Ser
|
|
ENST00000625216.2:c.161T>C
|
ENSP00000486898.1:p.Phe54Ser
|
|
ENST00000627232.2:c.903T>C
|
ENSP00000486037.1:n.903T>C
|
|
ENST00000627317.1:c.604T>C
|
|
|
ENST00000629179.1:n.754T>C
|
|
|
ENST00000631020.2:c.875T>C
|
ENSP00000486707.1:p.Phe292Ser
|
|
NM_007254.3:c.983T>C
|
NP_009185.2:p.Phe328Ser
|
|
NM_007254.4:c.983T>C
MANE Select
|
NP_009185.2:p.Phe328Ser
|
|