ENST00000373344.11:c.7262A>G
MANE Select
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ENSP00000362441.4:p.Gln2421Arg
|
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ENST00000675732.1:c.2360A>G
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ENSP00000502598.1:p.Gln787Arg
|
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ENST00000373344.9:c.7262A>G
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ENSP00000362441.4:p.Gln2421Arg
|
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ENST00000395603.7:c.7148A>G
|
ENSP00000378967.3:p.Gln2383Arg
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ENST00000480283.5:c.*6890A>G
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ENSP00000480196.1:n.*6890A>G
|
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ENST00000623706.3:n.5582A>G
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|
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ENST00000624766.1:n.493A>G
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|
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NM_000489.4:c.7262A>G
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NP_000480.3:p.Gln2421Arg
|
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NM_138270.3:c.7148A>G
|
NP_612114.2:p.Gln2383Arg
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XM_005262153.3:c.7259A>G
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XP_005262210.2:p.Gln2420Arg
|
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XM_005262154.3:c.7175A>G
|
XP_005262211.2:p.Gln2392Arg
|
|
XM_005262155.3:c.7145A>G
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XP_005262212.2:p.Gln2382Arg
|
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XM_005262156.3:c.7097A>G
|
XP_005262213.2:p.Gln2366Arg
|
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XM_005262157.3:c.7058A>G
|
XP_005262214.2:p.Gln2353Arg
|
|
XM_006724666.2:c.7145A>G
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XP_006724729.1:p.Gln2382Arg
|
|
XM_006724667.2:c.6983A>G
|
XP_006724730.1:p.Gln2328Arg
|
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XR_938400.1:n.8854A>G
|
|
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NM_000489.5:c.7262A>G
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NP_000480.3:p.Gln2421Arg
|
|
XM_005262153.5:c.7259A>G
|
XP_005262210.2:p.Gln2420Arg
|
|
XM_005262154.5:c.7175A>G
|
XP_005262211.2:p.Gln2392Arg
|
|
XM_005262155.4:c.7145A>G
|
XP_005262212.2:p.Gln2382Arg
|
|
XM_005262156.4:c.7097A>G
|
XP_005262213.2:p.Gln2366Arg
|
|
XM_005262157.5:c.7058A>G
|
XP_005262214.2:p.Gln2353Arg
|
|
XM_006724666.4:c.7145A>G
|
XP_006724729.1:p.Gln2382Arg
|
|
XM_006724667.3:c.6983A>G
|
XP_006724730.1:p.Gln2328Arg
|
|
XM_017029601.2:c.7172A>G
|
XP_016885090.1:p.Gln2391Arg
|
|
XM_017029602.1:c.7142A>G
|
XP_016885091.1:p.Gln2381Arg
|
|
XM_017029603.1:c.7094A>G
|
XP_016885092.1:p.Gln2365Arg
|
|
XM_017029604.2:c.7061A>G
|
XP_016885093.1:p.Gln2354Arg
|
|
XM_017029605.1:c.7058A>G
|
XP_016885094.1:p.Gln2353Arg
|
|
XM_017029606.2:c.7031A>G
|
XP_016885095.1:p.Gln2344Arg
|
|
XM_017029607.2:c.7028A>G
|
XP_016885096.1:p.Gln2343Arg
|
|
XM_017029608.2:c.6980A>G
|
XP_016885097.1:p.Gln2327Arg
|
|
XM_017029609.1:c.6944A>G
|
XP_016885098.1:p.Gln2315Arg
|
|
XM_017029610.1:c.6941A>G
|
XP_016885099.1:p.Gln2314Arg
|
|
XM_017029611.1:c.6896A>G
|
XP_016885100.1:p.Gln2299Arg
|
|
XR_001755700.2:n.7561A>G
|
|
|
NM_138270.4:c.7148A>G
|
NP_612114.2:p.Gln2383Arg
|
|
NM_000489.6:c.7262A>G
MANE Select
|
NP_000480.3:p.Gln2421Arg
|
|
NM_138270.5:c.7148A>G
|
NP_612114.2:p.Gln2383Arg
|
|