ENST00000373344.11:c.7446A>G
MANE Select
|
ENSP00000362441.4:p.Lys2482=
|
|
ENST00000675732.1:c.2544A>G
|
ENSP00000502598.1:p.Lys848=
|
|
ENST00000373344.9:c.7446A>G
|
ENSP00000362441.4:p.Lys2482=
|
|
ENST00000395603.7:c.7332A>G
|
ENSP00000378967.3:p.Lys2444=
|
|
ENST00000480283.5:c.*7074A>G
|
ENSP00000480196.1:n.*7074A>G
|
|
ENST00000623706.3:n.5766A>G
|
|
|
NM_000489.4:c.7446A>G
|
NP_000480.3:p.Lys2482=
|
|
NM_138270.3:c.7332A>G
|
NP_612114.2:p.Lys2444=
|
|
XM_005262153.3:c.7443A>G
|
XP_005262210.2:p.Lys2481=
|
|
XM_005262154.3:c.7359A>G
|
XP_005262211.2:p.Lys2453=
|
|
XM_005262155.3:c.7329A>G
|
XP_005262212.2:p.Lys2443=
|
|
XM_005262156.3:c.7281A>G
|
XP_005262213.2:p.Lys2427=
|
|
XM_005262157.3:c.7242A>G
|
XP_005262214.2:p.Lys2414=
|
|
XM_006724666.2:c.7329A>G
|
XP_006724729.1:p.Lys2443=
|
|
XM_006724667.2:c.7167A>G
|
XP_006724730.1:p.Lys2389=
|
|
XR_938400.1:n.9038A>G
|
|
|
NM_000489.5:c.7446A>G
|
NP_000480.3:p.Lys2482=
|
|
XM_005262153.5:c.7443A>G
|
XP_005262210.2:p.Lys2481=
|
|
XM_005262154.5:c.7359A>G
|
XP_005262211.2:p.Lys2453=
|
|
XM_005262155.4:c.7329A>G
|
XP_005262212.2:p.Lys2443=
|
|
XM_005262156.4:c.7281A>G
|
XP_005262213.2:p.Lys2427=
|
|
XM_005262157.5:c.7242A>G
|
XP_005262214.2:p.Lys2414=
|
|
XM_006724666.4:c.7329A>G
|
XP_006724729.1:p.Lys2443=
|
|
XM_006724667.3:c.7167A>G
|
XP_006724730.1:p.Lys2389=
|
|
XM_017029601.2:c.7356A>G
|
XP_016885090.1:p.Lys2452=
|
|
XM_017029602.1:c.7326A>G
|
XP_016885091.1:p.Lys2442=
|
|
XM_017029603.1:c.7278A>G
|
XP_016885092.1:p.Lys2426=
|
|
XM_017029604.2:c.7245A>G
|
XP_016885093.1:p.Lys2415=
|
|
XM_017029605.1:c.7242A>G
|
XP_016885094.1:p.Lys2414=
|
|
XM_017029606.2:c.7215A>G
|
XP_016885095.1:p.Lys2405=
|
|
XM_017029607.2:c.7212A>G
|
XP_016885096.1:p.Lys2404=
|
|
XM_017029608.2:c.7164A>G
|
XP_016885097.1:p.Lys2388=
|
|
XM_017029609.1:c.7128A>G
|
XP_016885098.1:p.Lys2376=
|
|
XM_017029610.1:c.7125A>G
|
XP_016885099.1:p.Lys2375=
|
|
XM_017029611.1:c.7080A>G
|
XP_016885100.1:p.Lys2360=
|
|
XR_001755700.2:n.7745A>G
|
|
|
NM_138270.4:c.7332A>G
|
NP_612114.2:p.Lys2444=
|
|
NM_000489.6:c.7446A>G
MANE Select
|
NP_000480.3:p.Lys2482=
|
|
NM_138270.5:c.7332A>G
|
NP_612114.2:p.Lys2444=
|
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