ENST00000456935.7:c.1822G>T
MANE Select
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ENSP00000395473.2:p.Glu608Ter
|
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ENST00000221363.8:c.1819G>T
|
ENSP00000221363.4:p.Glu607Ter
|
|
ENST00000433513.5:n.428G>T
|
|
|
ENST00000456935.6:c.1822G>T
|
ENSP00000395473.2:p.Glu608Ter
|
|
ENST00000466794.5:n.2412G>T
|
|
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ENST00000593686.1:c.415G>T
|
|
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ENST00000595880.5:n.419G>T
|
|
|
ENST00000596591.1:c.186G>T
|
|
|
NM_000528.3:c.1822G>T
|
NP_000519.2:p.Glu608Ter
|
|
NM_001173498.1:c.1819G>T
|
NP_001166969.1:p.Glu607Ter
|
|
XM_005259913.1:c.1825G>T
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XP_005259970.1:p.Glu609Ter
|
|
XM_011528017.1:c.721G>T
|
XP_011526319.1:p.Glu241Ter
|
|
XM_005259913.2:c.1825G>T
|
XP_005259970.1:p.Glu609Ter
|
|
XM_024451518.1:c.721G>T
|
XP_024307286.1:p.Glu241Ter
|
|
NM_000528.4:c.1822G>T
MANE Select
|
NP_000519.2:p.Glu608Ter
|
|
NM_001173498.2:c.1819G>T
|
NP_001166969.1:p.Glu607Ter
|
|