ENST00000373344.11:c.6258A>T
MANE Select
|
ENSP00000362441.4:p.Leu2086Phe
|
|
ENST00000636152.1:n.93A>T
|
|
|
ENST00000675732.1:c.1356A>T
|
ENSP00000502598.1:p.Leu452Phe
|
|
ENST00000373344.9:c.6258A>T
|
ENSP00000362441.4:p.Leu2086Phe
|
|
ENST00000395603.7:c.6144A>T
|
ENSP00000378967.3:p.Leu2048Phe
|
|
ENST00000480283.5:c.*5886A>T
|
ENSP00000480196.1:n.*5886A>T
|
|
ENST00000623316.1:c.742A>T
|
|
|
ENST00000623706.3:n.3328A>T
|
|
|
NM_000489.4:c.6258A>T
|
NP_000480.3:p.Leu2086Phe
|
|
NM_138270.3:c.6144A>T
|
NP_612114.2:p.Leu2048Phe
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|
XM_005262153.3:c.6255A>T
|
XP_005262210.2:p.Leu2085Phe
|
|
XM_005262154.3:c.6171A>T
|
XP_005262211.2:p.Leu2057Phe
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|
XM_005262155.3:c.6141A>T
|
XP_005262212.2:p.Leu2047Phe
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|
XM_005262156.3:c.6093A>T
|
XP_005262213.2:p.Leu2031Phe
|
|
XM_005262157.3:c.6054A>T
|
XP_005262214.2:p.Leu2018Phe
|
|
XM_006724666.2:c.6141A>T
|
XP_006724729.1:p.Leu2047Phe
|
|
XM_006724667.2:c.5979A>T
|
XP_006724730.1:p.Leu1993Phe
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|
XR_938400.1:n.6600A>T
|
|
|
NM_000489.5:c.6258A>T
|
NP_000480.3:p.Leu2086Phe
|
|
XM_005262153.5:c.6255A>T
|
XP_005262210.2:p.Leu2085Phe
|
|
XM_005262154.5:c.6171A>T
|
XP_005262211.2:p.Leu2057Phe
|
|
XM_005262155.4:c.6141A>T
|
XP_005262212.2:p.Leu2047Phe
|
|
XM_005262156.4:c.6093A>T
|
XP_005262213.2:p.Leu2031Phe
|
|
XM_005262157.5:c.6054A>T
|
XP_005262214.2:p.Leu2018Phe
|
|
XM_006724666.4:c.6141A>T
|
XP_006724729.1:p.Leu2047Phe
|
|
XM_006724667.3:c.5979A>T
|
XP_006724730.1:p.Leu1993Phe
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|
XM_017029601.2:c.6168A>T
|
XP_016885090.1:p.Leu2056Phe
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|
XM_017029602.1:c.6138A>T
|
XP_016885091.1:p.Leu2046Phe
|
|
XM_017029603.1:c.6090A>T
|
XP_016885092.1:p.Leu2030Phe
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|
XM_017029604.2:c.6057A>T
|
XP_016885093.1:p.Leu2019Phe
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|
XM_017029605.1:c.6054A>T
|
XP_016885094.1:p.Leu2018Phe
|
|
XM_017029606.2:c.6027A>T
|
XP_016885095.1:p.Leu2009Phe
|
|
XM_017029607.2:c.6024A>T
|
XP_016885096.1:p.Leu2008Phe
|
|
XM_017029608.2:c.5976A>T
|
XP_016885097.1:p.Leu1992Phe
|
|
XM_017029609.1:c.5940A>T
|
XP_016885098.1:p.Leu1980Phe
|
|
XM_017029610.1:c.5937A>T
|
XP_016885099.1:p.Leu1979Phe
|
|
XM_017029611.1:c.5892A>T
|
XP_016885100.1:p.Leu1964Phe
|
|
XR_001755700.2:n.6557A>T
|
|
|
NM_138270.4:c.6144A>T
|
NP_612114.2:p.Leu2048Phe
|
|
NM_000489.6:c.6258A>T
MANE Select
|
NP_000480.3:p.Leu2086Phe
|
|
NM_138270.5:c.6144A>T
|
NP_612114.2:p.Leu2048Phe
|
|