ENST00000373344.11:c.7379A>T
MANE Select
|
ENSP00000362441.4:p.Tyr2460Phe
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|
ENST00000675732.1:c.2477A>T
|
ENSP00000502598.1:p.Tyr826Phe
|
|
ENST00000373344.9:c.7379A>T
|
ENSP00000362441.4:p.Tyr2460Phe
|
|
ENST00000395603.7:c.7265A>T
|
ENSP00000378967.3:p.Tyr2422Phe
|
|
ENST00000480283.5:c.*7007A>T
|
ENSP00000480196.1:n.*7007A>T
|
|
ENST00000623706.3:n.5699A>T
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|
|
NM_000489.4:c.7379A>T
|
NP_000480.3:p.Tyr2460Phe
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|
NM_138270.3:c.7265A>T
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NP_612114.2:p.Tyr2422Phe
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|
XM_005262153.3:c.7376A>T
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XP_005262210.2:p.Tyr2459Phe
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XM_005262154.3:c.7292A>T
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XP_005262211.2:p.Tyr2431Phe
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|
XM_005262155.3:c.7262A>T
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XP_005262212.2:p.Tyr2421Phe
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XM_005262156.3:c.7214A>T
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XP_005262213.2:p.Tyr2405Phe
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|
XM_005262157.3:c.7175A>T
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XP_005262214.2:p.Tyr2392Phe
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|
XM_006724666.2:c.7262A>T
|
XP_006724729.1:p.Tyr2421Phe
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|
XM_006724667.2:c.7100A>T
|
XP_006724730.1:p.Tyr2367Phe
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|
XR_938400.1:n.8971A>T
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|
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NM_000489.5:c.7379A>T
|
NP_000480.3:p.Tyr2460Phe
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|
XM_005262153.5:c.7376A>T
|
XP_005262210.2:p.Tyr2459Phe
|
|
XM_005262154.5:c.7292A>T
|
XP_005262211.2:p.Tyr2431Phe
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|
XM_005262155.4:c.7262A>T
|
XP_005262212.2:p.Tyr2421Phe
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|
XM_005262156.4:c.7214A>T
|
XP_005262213.2:p.Tyr2405Phe
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|
XM_005262157.5:c.7175A>T
|
XP_005262214.2:p.Tyr2392Phe
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|
XM_006724666.4:c.7262A>T
|
XP_006724729.1:p.Tyr2421Phe
|
|
XM_006724667.3:c.7100A>T
|
XP_006724730.1:p.Tyr2367Phe
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|
XM_017029601.2:c.7289A>T
|
XP_016885090.1:p.Tyr2430Phe
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|
XM_017029602.1:c.7259A>T
|
XP_016885091.1:p.Tyr2420Phe
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|
XM_017029603.1:c.7211A>T
|
XP_016885092.1:p.Tyr2404Phe
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|
XM_017029604.2:c.7178A>T
|
XP_016885093.1:p.Tyr2393Phe
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|
XM_017029605.1:c.7175A>T
|
XP_016885094.1:p.Tyr2392Phe
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|
XM_017029606.2:c.7148A>T
|
XP_016885095.1:p.Tyr2383Phe
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|
XM_017029607.2:c.7145A>T
|
XP_016885096.1:p.Tyr2382Phe
|
|
XM_017029608.2:c.7097A>T
|
XP_016885097.1:p.Tyr2366Phe
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|
XM_017029609.1:c.7061A>T
|
XP_016885098.1:p.Tyr2354Phe
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|
XM_017029610.1:c.7058A>T
|
XP_016885099.1:p.Tyr2353Phe
|
|
XM_017029611.1:c.7013A>T
|
XP_016885100.1:p.Tyr2338Phe
|
|
XR_001755700.2:n.7678A>T
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|
|
NM_138270.4:c.7265A>T
|
NP_612114.2:p.Tyr2422Phe
|
|
NM_000489.6:c.7379A>T
MANE Select
|
NP_000480.3:p.Tyr2460Phe
|
|
NM_138270.5:c.7265A>T
|
NP_612114.2:p.Tyr2422Phe
|
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