ENST00000541562.6:c.2399G=
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ENSP00000441000.2:p.Arg800=
|
|
ENST00000672801.1:c.2393G=
|
ENSP00000500615.1:p.Arg798=
|
|
ENST00000676266.1:c.2399G=
MANE Select
|
ENSP00000502585.1:p.Arg800=
|
|
ENST00000321897.9:c.2399G=
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ENSP00000316092.5:p.Arg800=
|
|
ENST00000469358.5:n.2387G=
|
|
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ENST00000473916.1:n.110G=
|
|
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ENST00000476162.5:n.1186G=
|
|
|
ENST00000477052.1:n.485G=
|
|
|
ENST00000477288.5:n.5012G=
|
|
|
ENST00000541562.5:c.2489G=
|
ENSP00000441000.1:p.Arg830=
|
|
ENST00000542001.5:c.2393G=
|
ENSP00000438200.2:p.Arg798=
|
|
ENST00000625423.2:c.1979G=
|
ENSP00000485818.1:p.Arg660=
|
|
NM_001167733.2:c.1979G=
|
NP_001161205.1:p.Arg660=
|
|
NM_001167734.1:c.2489G=
|
NP_001161206.1:p.Arg830=
|
|
NM_020442.5:c.2399G=
|
NP_065175.4:p.Arg800=
|
|
NM_001167733.3:c.1979G=
|
NP_001161205.1:p.Arg660=
|
|
NM_001167734.2:c.2489G=
|
NP_001161206.1:p.Arg830=
|
|
NM_020442.6:c.2399G=
MANE Select
|
NP_065175.4:p.Arg800=
|
|