ENST00000356231.4:c.2133_2134delinsAT
MANE Select
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ENSP00000348564.3:p.Glu711=
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ENST00000643434.1:c.*1311_*1312delinsAT
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ENSP00000494699.1:n.*1311_*1312delinsAT
|
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ENST00000356231.3:c.2133_2134delinsAT
|
ENSP00000348564.3:p.Glu711=
|
|
ENST00000562465.5:c.126_127delinsAT
|
ENSP00000454246.1:p.Glu42=
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NM_138477.2:c.2133_2134delinsAT
|
NP_612486.2:p.Glu711=
|
|
XM_005254176.3:c.2136_2137delinsAT
|
XP_005254233.1:p.Glu712=
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|
XM_011521270.1:c.2160_2161delinsAT
|
XP_011519572.1:p.Glu720=
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|
XM_011521271.1:c.2157_2158delinsAT
|
XP_011519573.1:p.Glu719=
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|
XM_011521272.1:c.2160_2161delinsAT
|
XP_011519574.1:p.Glu720=
|
|
XM_011521273.1:c.2160_2161delinsAT
|
XP_011519575.1:p.Glu720=
|
|
XM_011521274.1:c.1125_1126delinsAT
|
XP_011519576.1:p.Glu375=
|
|
XM_011521275.1:c.1377_1378delinsAT
|
XP_011519577.1:p.Glu459=
|
|
XR_931757.1:n.2133_2134delinsAT
|
|
|
NM_138477.4:c.2133_2134delinsAT
MANE Select
|
NP_612486.2:p.Glu711=
|
|
XM_005254176.5:c.2136_2137delinsAT
|
XP_005254233.1:p.Glu712=
|
|
XM_011521270.2:c.2160_2161delinsAT
|
XP_011519572.1:p.Glu720=
|
|
XM_011521271.2:c.2157_2158delinsAT
|
XP_011519573.1:p.Glu719=
|
|
XM_011521274.2:c.1125_1126delinsAT
|
XP_011519576.1:p.Glu375=
|
|
XR_001751104.1:n.2190_2191delinsAT
|
|
|
XR_001751105.1:n.2190_2191delinsAT
|
|
|
XR_931757.2:n.2153_2154delinsAT
|
|
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