ENST00000261304.7:c.226G>T
MANE Select
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ENSP00000261304.2:p.Glu76Ter
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ENST00000261304.6:c.226G>T
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ENSP00000261304.2:p.Glu76Ter
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ENST00000393568.8:c.196-286G>T
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ENSP00000377198.4:n.196-286G>T
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ENST00000393569.6:c.148G>T
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ENSP00000377199.2:p.Glu50Ter
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ENST00000474294.6:n.216G>T
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|
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ENST00000544807.6:c.58G>T
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ENSP00000437513.2:p.Glu20Ter
|
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ENST00000554372.5:c.226G>T
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ENSP00000451884.1:p.Glu76Ter
|
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ENST00000554916.5:n.105G>T
|
|
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ENST00000555956.1:n.31G>T
|
|
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ENST00000556879.5:c.286G>T
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ENSP00000452208.1:n.286G>T
|
|
ENST00000557316.5:c.226G>T
|
ENSP00000452314.1:p.Glu76Ter
|
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ENST00000622264.4:c.216G>T
|
|
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NM_000153.3:c.226G>T
|
NP_000144.2:p.Glu76Ter
|
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NM_001201401.1:c.196-286G>T
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NP_001188330.1:n.196-286G>T
|
|
NM_001201402.1:c.148G>T
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NP_001188331.1:p.Glu50Ter
|
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XM_011536618.1:c.58G>T
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XP_011534920.1:p.Glu20Ter
|
|
XM_011536618.2:c.58G>T
|
XP_011534920.1:p.Glu20Ter
|
|
NM_000153.4:c.226G>T
MANE Select
|
NP_000144.2:p.Glu76Ter
|
|
NM_001201401.2:c.196-286G>T
|
NP_001188330.1:n.196-286G>T
|
|
NM_001201402.2:c.148G>T
|
NP_001188331.1:p.Glu50Ter
|
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