ENST00000373344.11:c.7191A>C
MANE Select
|
ENSP00000362441.4:p.Lys2397Asn
|
|
ENST00000675732.1:c.2289A>C
|
ENSP00000502598.1:p.Lys763Asn
|
|
ENST00000373344.9:c.7191A>C
|
ENSP00000362441.4:p.Lys2397Asn
|
|
ENST00000395603.7:c.7077A>C
|
ENSP00000378967.3:p.Lys2359Asn
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ENST00000480283.5:c.*6819A>C
|
ENSP00000480196.1:n.*6819A>C
|
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ENST00000623706.3:n.5511A>C
|
|
|
ENST00000624766.1:n.422A>C
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|
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NM_000489.4:c.7191A>C
|
NP_000480.3:p.Lys2397Asn
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|
NM_138270.3:c.7077A>C
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NP_612114.2:p.Lys2359Asn
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|
XM_005262153.3:c.7188A>C
|
XP_005262210.2:p.Lys2396Asn
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XM_005262154.3:c.7104A>C
|
XP_005262211.2:p.Lys2368Asn
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XM_005262155.3:c.7074A>C
|
XP_005262212.2:p.Lys2358Asn
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XM_005262156.3:c.7026A>C
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XP_005262213.2:p.Lys2342Asn
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|
XM_005262157.3:c.6987A>C
|
XP_005262214.2:p.Lys2329Asn
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XM_006724666.2:c.7074A>C
|
XP_006724729.1:p.Lys2358Asn
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|
XM_006724667.2:c.6912A>C
|
XP_006724730.1:p.Lys2304Asn
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|
XR_938400.1:n.8783A>C
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|
|
NM_000489.5:c.7191A>C
|
NP_000480.3:p.Lys2397Asn
|
|
XM_005262153.5:c.7188A>C
|
XP_005262210.2:p.Lys2396Asn
|
|
XM_005262154.5:c.7104A>C
|
XP_005262211.2:p.Lys2368Asn
|
|
XM_005262155.4:c.7074A>C
|
XP_005262212.2:p.Lys2358Asn
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|
XM_005262156.4:c.7026A>C
|
XP_005262213.2:p.Lys2342Asn
|
|
XM_005262157.5:c.6987A>C
|
XP_005262214.2:p.Lys2329Asn
|
|
XM_006724666.4:c.7074A>C
|
XP_006724729.1:p.Lys2358Asn
|
|
XM_006724667.3:c.6912A>C
|
XP_006724730.1:p.Lys2304Asn
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|
XM_017029601.2:c.7101A>C
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XP_016885090.1:p.Lys2367Asn
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|
XM_017029602.1:c.7071A>C
|
XP_016885091.1:p.Lys2357Asn
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|
XM_017029603.1:c.7023A>C
|
XP_016885092.1:p.Lys2341Asn
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|
XM_017029604.2:c.6990A>C
|
XP_016885093.1:p.Lys2330Asn
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XM_017029605.1:c.6987A>C
|
XP_016885094.1:p.Lys2329Asn
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|
XM_017029606.2:c.6960A>C
|
XP_016885095.1:p.Lys2320Asn
|
|
XM_017029607.2:c.6957A>C
|
XP_016885096.1:p.Lys2319Asn
|
|
XM_017029608.2:c.6909A>C
|
XP_016885097.1:p.Lys2303Asn
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|
XM_017029609.1:c.6873A>C
|
XP_016885098.1:p.Lys2291Asn
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|
XM_017029610.1:c.6870A>C
|
XP_016885099.1:p.Lys2290Asn
|
|
XM_017029611.1:c.6825A>C
|
XP_016885100.1:p.Lys2275Asn
|
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XR_001755700.2:n.7490A>C
|
|
|
NM_138270.4:c.7077A>C
|
NP_612114.2:p.Lys2359Asn
|
|
NM_000489.6:c.7191A>C
MANE Select
|
NP_000480.3:p.Lys2397Asn
|
|
NM_138270.5:c.7077A>C
|
NP_612114.2:p.Lys2359Asn
|
|