ENST00000255078.8:c.1884G>A
MANE Select
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ENSP00000255078.4:p.Glu628=
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ENST00000674675.1:c.128G>A
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ENST00000674878.1:c.128G>A
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ENST00000674955.1:c.*601G>A
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ENSP00000502463.1:n.*601G>A
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ENST00000675118.1:c.1372G>A
|
|
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ENST00000675389.1:n.159G>A
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|
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ENST00000675615.1:c.1884G>A
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ENSP00000502413.1:p.Glu628=
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ENST00000675648.1:n.1259G>A
|
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ENST00000675916.1:c.128G>A
|
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ENST00000676173.1:n.2629G>A
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ENST00000676182.1:c.315G>A
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ENST00000676228.1:c.*1207G>A
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ENSP00000502375.1:n.*1207G>A
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ENST00000255078.7:c.1884G>A
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ENSP00000255078.3:p.Glu628=
|
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ENST00000539064.5:n.1643G>A
|
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ENST00000543739.5:n.877G>A
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ENST00000545475.1:n.480G>A
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NM_002180.2:c.1884G>A , LRG_250t1:c.1884G>A
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NP_002171.2:p.Glu628=
|
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XM_005273974.2:c.873G>A
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XP_005274031.1:p.Glu291=
|
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XM_005273975.2:c.756G>A
|
XP_005274032.1:p.Glu252=
|
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XM_011544994.1:c.651G>A
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XP_011543296.1:p.Glu217=
|
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XR_949903.1:n.1986G>A
|
|
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XM_005273975.3:c.756G>A
|
XP_005274032.1:p.Glu252=
|
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XM_017017669.2:c.873G>A
|
XP_016873158.1:p.Glu291=
|
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XM_017017670.2:c.873G>A
|
XP_016873159.1:p.Glu291=
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XR_949903.3:n.1982G>A
|
|
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NM_002180.3:c.1884G>A
MANE Select
|
NP_002171.2:p.Glu628=
|
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