ENST00000380707.9:c.843A>C
MANE Select
|
ENSP00000370083.4:p.Arg281Ser
|
|
ENST00000351205.8:c.843A>C
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ENSP00000305857.5:p.Arg281Ser
|
|
ENST00000380707.8:c.843A>C
|
ENSP00000370083.4:p.Arg281Ser
|
|
ENST00000503079.6:c.747A>C
|
ENSP00000428128.1:p.Arg249Ser
|
|
ENST00000506163.5:c.835-490A>C
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ENSP00000424926.1:n.835-490A>C
|
|
ENST00000506239.6:c.*59-490A>C
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ENSP00000422679.2:n.*59-490A>C
|
|
ENST00000510679.1:n.97A>C
|
|
|
ENST00000514951.5:c.642A>C
|
ENSP00000423298.1:p.Arg214Ser
|
|
NM_000344.3:c.843A>C , LRG_676t1:c.843A>C
|
NP_000335.1:p.Arg281Ser
|
|
NM_001297715.1:c.835-490A>C
|
NP_001284644.1:n.835-490A>C
|
|
NM_022874.2:c.747A>C
|
NP_075012.1:p.Arg249Ser
|
|
XM_011543597.1:c.642A>C
|
XP_011541899.1:p.Arg214Ser
|
|
XM_011543598.1:c.546A>C
|
XP_011541900.1:p.Arg182Ser
|
|
XM_011543598.3:c.546A>C
|
XP_011541900.1:p.Arg182Ser
|
|
XM_017009786.1:c.739-490A>C
|
XP_016865275.1:n.739-490A>C
|
|
NM_000344.4:c.843A>C
MANE Select
|
NP_000335.1:p.Arg281Ser
|
|