ENST00000352909.8:c.797A>T
MANE Select
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ENSP00000325951.4:p.Glu266Val
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ENST00000324155.8:c.*486A>T
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ENSP00000325831.3:n.*486A>T
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|
ENST00000333684.9:c.696-382A>T
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ENSP00000328814.6:n.696-382A>T
|
|
ENST00000352909.7:c.797A>T
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ENSP00000325951.3:p.Glu266Val
|
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ENST00000381168.7:c.*517A>T
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ENSP00000370560.3:n.*517A>T
|
|
ENST00000381175.5:c.878A>T
|
ENSP00000370567.1:p.Glu293Val
|
|
ENST00000381178.5:c.890A>T
|
ENSP00000370571.1:p.Glu297Val
|
|
ENST00000412076.1:c.136-382A>T
|
|
|
ENST00000416223.5:c.136-163A>T
|
|
|
ENST00000469226.1:n.926A>T
|
|
|
ENST00000479437.5:n.346A>T
|
|
|
NM_000360.3:c.797A>T
|
NP_000351.2:p.Glu266Val
|
|
NM_199292.2:c.890A>T
|
NP_954986.2:p.Glu297Val
|
|
NM_199293.2:c.878A>T
|
NP_954987.2:p.Glu293Val
|
|
XM_011520335.1:c.809A>T
|
XP_011518637.1:p.Glu270Val
|
|
XM_011520335.2:c.809A>T
|
XP_011518637.1:p.Glu270Val
|
|
NM_000360.4:c.797A>T
MANE Select
|
NP_000351.2:p.Glu266Val
|
|
NM_199292.3:c.890A>T
|
NP_954986.2:p.Glu297Val
|
|
NM_199293.3:c.878A>T
|
NP_954987.2:p.Glu293Val
|
|