ENST00000352480.10:c.823G=
MANE Select
|
ENSP00000253004.6:p.Gly275=
|
|
ENST00000352480.9:c.823G=
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ENSP00000253004.6:p.Gly275=
|
|
ENST00000372386.6:n.94G=
|
|
|
ENST00000372393.7:c.823G=
|
ENSP00000361469.2:p.Gly275=
|
|
ENST00000372394.5:c.823G=
|
ENSP00000361471.1:p.Gly275=
|
|
ENST00000470849.4:n.548G=
|
|
|
ENST00000492400.5:n.332G=
|
|
|
ENST00000493984.6:n.600G=
|
|
|
NM_000050.4:c.823G=
|
NP_000041.2:p.Gly275=
|
|
NM_054012.3:c.823G=
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NP_446464.1:p.Gly275=
|
|
XM_005272200.2:c.823G=
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XP_005272257.1:p.Gly275=
|
|
XM_011518705.1:c.937G=
|
XP_011517007.1:p.Gly313=
|
|
XM_005272200.3:c.823G=
|
XP_005272257.1:p.Gly275=
|
|
XM_011518705.2:c.937G=
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XP_011517007.1:p.Gly313=
|
|
XM_017014729.1:c.919G=
|
XP_016870218.1:p.Gly307=
|
|
NM_054012.4:c.823G=
MANE Select
|
NP_446464.1:p.Gly275=
|
|