ENST00000373344.11:c.7333A>T
MANE Select
|
ENSP00000362441.4:p.Ile2445Phe
|
|
ENST00000675732.1:c.2431A>T
|
ENSP00000502598.1:p.Ile811Phe
|
|
ENST00000373344.9:c.7333A>T
|
ENSP00000362441.4:p.Ile2445Phe
|
|
ENST00000395603.7:c.7219A>T
|
ENSP00000378967.3:p.Ile2407Phe
|
|
ENST00000480283.5:c.*6961A>T
|
ENSP00000480196.1:n.*6961A>T
|
|
ENST00000623706.3:n.5653A>T
|
|
|
ENST00000624766.1:n.564A>T
|
|
|
NM_000489.4:c.7333A>T
|
NP_000480.3:p.Ile2445Phe
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|
NM_138270.3:c.7219A>T
|
NP_612114.2:p.Ile2407Phe
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|
XM_005262153.3:c.7330A>T
|
XP_005262210.2:p.Ile2444Phe
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|
XM_005262154.3:c.7246A>T
|
XP_005262211.2:p.Ile2416Phe
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|
XM_005262155.3:c.7216A>T
|
XP_005262212.2:p.Ile2406Phe
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|
XM_005262156.3:c.7168A>T
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XP_005262213.2:p.Ile2390Phe
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|
XM_005262157.3:c.7129A>T
|
XP_005262214.2:p.Ile2377Phe
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|
XM_006724666.2:c.7216A>T
|
XP_006724729.1:p.Ile2406Phe
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|
XM_006724667.2:c.7054A>T
|
XP_006724730.1:p.Ile2352Phe
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|
XR_938400.1:n.8925A>T
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|
|
NM_000489.5:c.7333A>T
|
NP_000480.3:p.Ile2445Phe
|
|
XM_005262153.5:c.7330A>T
|
XP_005262210.2:p.Ile2444Phe
|
|
XM_005262154.5:c.7246A>T
|
XP_005262211.2:p.Ile2416Phe
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|
XM_005262155.4:c.7216A>T
|
XP_005262212.2:p.Ile2406Phe
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|
XM_005262156.4:c.7168A>T
|
XP_005262213.2:p.Ile2390Phe
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|
XM_005262157.5:c.7129A>T
|
XP_005262214.2:p.Ile2377Phe
|
|
XM_006724666.4:c.7216A>T
|
XP_006724729.1:p.Ile2406Phe
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|
XM_006724667.3:c.7054A>T
|
XP_006724730.1:p.Ile2352Phe
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|
XM_017029601.2:c.7243A>T
|
XP_016885090.1:p.Ile2415Phe
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|
XM_017029602.1:c.7213A>T
|
XP_016885091.1:p.Ile2405Phe
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|
XM_017029603.1:c.7165A>T
|
XP_016885092.1:p.Ile2389Phe
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|
XM_017029604.2:c.7132A>T
|
XP_016885093.1:p.Ile2378Phe
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|
XM_017029605.1:c.7129A>T
|
XP_016885094.1:p.Ile2377Phe
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|
XM_017029606.2:c.7102A>T
|
XP_016885095.1:p.Ile2368Phe
|
|
XM_017029607.2:c.7099A>T
|
XP_016885096.1:p.Ile2367Phe
|
|
XM_017029608.2:c.7051A>T
|
XP_016885097.1:p.Ile2351Phe
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|
XM_017029609.1:c.7015A>T
|
XP_016885098.1:p.Ile2339Phe
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|
XM_017029610.1:c.7012A>T
|
XP_016885099.1:p.Ile2338Phe
|
|
XM_017029611.1:c.6967A>T
|
XP_016885100.1:p.Ile2323Phe
|
|
XR_001755700.2:n.7632A>T
|
|
|
NM_138270.4:c.7219A>T
|
NP_612114.2:p.Ile2407Phe
|
|
NM_000489.6:c.7333A>T
MANE Select
|
NP_000480.3:p.Ile2445Phe
|
|
NM_138270.5:c.7219A>T
|
NP_612114.2:p.Ile2407Phe
|
|