ENST00000377443.7:c.406G>T
MANE Select
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ENSP00000366662.2:p.Glu136Ter
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ENST00000377436.6:c.406G>T
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ENSP00000366654.3:p.Glu136Ter
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|
ENST00000377442.3:c.226G>T
|
ENSP00000366661.2:p.Glu76Ter
|
|
ENST00000377443.6:c.406G>T
|
ENSP00000366662.2:p.Glu136Ter
|
|
ENST00000476083.1:n.99-1627G>T
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|
|
ENST00000549778.5:c.310G>T
|
ENSP00000447108.1:p.Glu104Ter
|
|
NM_001215.3:c.406G>T
|
NP_001206.2:p.Glu136Ter
|
|
NM_001270500.1:c.406G>T
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NP_001257429.1:p.Glu136Ter
|
|
NM_001270501.1:c.226G>T
|
NP_001257430.1:p.Glu76Ter
|
|
NM_001270502.1:c.25-1627G>T
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NP_001257431.1:n.25-1627G>T
|
|
XM_011542083.1:c.418G>T
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XP_011540385.1:p.Glu140Ter
|
|
XM_011542084.1:c.418G>T
|
XP_011540386.1:p.Glu140Ter
|
|
XM_011542083.3:c.418G>T
|
XP_011540385.1:p.Glu140Ter
|
|
XM_011542084.3:c.418G>T
|
XP_011540386.1:p.Glu140Ter
|
|
NM_001215.4:c.406G>T
MANE Select
|
NP_001206.2:p.Glu136Ter
|
|
NM_001270500.2:c.406G>T
|
NP_001257429.1:p.Glu136Ter
|
|
NM_001270501.2:c.226G>T
|
NP_001257430.1:p.Glu76Ter
|
|
NM_001270502.2:c.25-1627G>T
|
NP_001257431.1:n.25-1627G>T
|
|