ENST00000352410.9:c.707A>T
MANE Select
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ENSP00000318318.6:p.Glu236Val
|
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ENST00000323744.10:c.524A>T
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ENSP00000318192.6:p.Glu175Val
|
|
ENST00000352410.8:c.707A>T
|
ENSP00000318318.6:p.Glu236Val
|
|
ENST00000535694.5:c.557A>T
|
ENSP00000440447.1:p.Glu186Val
|
|
ENST00000561470.5:c.*603A>T
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ENSP00000454267.1:n.*603A>T
|
|
ENST00000562606.5:c.647A>T
|
ENSP00000457020.1:p.Glu216Val
|
|
ENST00000562800.5:c.256-1351A>T
|
ENSP00000457619.1:n.256-1351A>T
|
|
ENST00000563422.5:c.707A>T
|
ENSP00000457885.1:p.Glu236Val
|
|
ENST00000563786.5:c.647A>T
|
ENSP00000455241.1:p.Glu216Val
|
|
ENST00000564003.5:c.374A>T
|
ENSP00000454312.1:p.Glu125Val
|
|
ENST00000566377.5:c.707A>T
|
ENSP00000455405.1:p.Glu236Val
|
|
ENST00000566556.1:n.755A>T
|
|
|
ENST00000567177.1:c.485A>T
|
ENSP00000457013.1:p.Glu162Val
|
|
ENST00000569931.5:c.647A>T
|
ENSP00000455161.1:p.Glu216Val
|
|
NM_001289155.1:c.707A>T
|
NP_001276084.1:p.Glu236Val
|
|
NM_001289156.1:c.557A>T
|
NP_001276085.1:p.Glu186Val
|
|
NM_001289157.1:c.524A>T
|
NP_001276086.1:p.Glu175Val
|
|
NM_002435.2:c.707A>T
|
NP_002426.1:p.Glu236Val
|
|
XM_011521592.1:c.695A>T
|
XP_011519894.1:p.Glu232Val
|
|
XM_011521593.1:c.647A>T
|
XP_011519895.1:p.Glu216Val
|
|
NM_001330372.1:c.647A>T
|
NP_001317301.1:p.Glu216Val
|
|
XM_017022208.1:c.647A>T
|
XP_016877697.1:p.Glu216Val
|
|
XM_017022209.2:c.557A>T
|
XP_016877698.1:p.Glu186Val
|
|
NM_002435.3:c.707A>T
MANE Select
|
NP_002426.1:p.Glu236Val
|
|
NM_001289155.2:c.707A>T
|
NP_001276084.1:p.Glu236Val
|
|
NM_001289156.2:c.557A>T
|
NP_001276085.1:p.Glu186Val
|
|
NM_001289157.2:c.524A>T
|
NP_001276086.1:p.Glu175Val
|
|
NM_001330372.2:c.647A>T
|
NP_001317301.1:p.Glu216Val
|
|