ENST00000333213.11:c.542A>T
MANE Select
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ENSP00000327487.6:p.Glu181Val
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ENST00000434205.8:c.239A>T
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ENSP00000406559.4:p.Glu80Val
|
|
ENST00000545228.3:c.542A>T
|
ENSP00000438169.3:p.Glu181Val
|
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ENST00000579449.2:n.341A>T
|
|
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ENST00000580013.6:n.551A>T
|
|
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ENST00000583818.2:c.596A>T
|
ENSP00000461928.2:n.596A>T
|
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ENST00000679370.1:n.929A>T
|
|
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ENST00000679429.1:c.534A>T
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ENSP00000505403.1:p.Ter178Cys
|
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ENST00000679443.1:n.417A>T
|
|
|
ENST00000679782.1:c.542A>T
|
ENSP00000505995.1:p.Glu181Val
|
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ENST00000679919.1:n.417A>T
|
|
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ENST00000679928.1:c.*153A>T
|
ENSP00000506071.1:n.*153A>T
|
|
ENST00000680528.1:n.567A>T
|
|
|
ENST00000680999.1:c.542A>T
|
ENSP00000504984.1:p.Glu181Val
|
|
ENST00000681282.1:c.542A>T
|
ENSP00000506339.1:p.Glu181Val
|
|
ENST00000333213.10:c.542A>T
|
ENSP00000327487.6:p.Glu181Val
|
|
ENST00000578415.1:c.502A>T
|
|
|
ENST00000580013.5:n.559A>T
|
|
|
ENST00000583173.5:c.377A>T
|
ENSP00000463619.1:p.Glu126Val
|
|
ENST00000583818.1:c.491A>T
|
ENSP00000461928.1:n.491A>T
|
|
NM_207346.2:c.542A>T
|
NP_997229.2:p.Glu181Val
|
|
XM_005257229.2:c.542A>T
|
XP_005257286.1:p.Glu181Val
|
|
XM_006721821.2:c.239A>T
|
XP_006721884.1:p.Glu80Val
|
|
XM_011524616.1:c.542A>T
|
XP_011522918.1:p.Glu181Val
|
|
XM_011524617.1:c.542A>T
|
XP_011522919.1:p.Glu181Val
|
|
XM_011524618.1:c.542A>T
|
XP_011522920.1:p.Glu181Val
|
|
XR_243646.2:n.572A>T
|
|
|
XM_005257229.4:c.542A>T
|
XP_005257286.1:p.Glu181Val
|
|
XR_243646.4:n.578A>T
|
|
|
NM_207346.3:c.542A>T
MANE Select
|
NP_997229.2:p.Glu181Val
|
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