ENST00000324001.8:c.2201A>T
MANE Select
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ENSP00000326018.6:p.Glu734Val
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ENST00000673881.1:c.1784A>T
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ENSP00000501070.1:p.Glu595Val
|
|
ENST00000674005.2:c.2486A>T
|
ENSP00000501261.1:p.Glu829Val
|
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ENST00000674773.1:c.1784A>T
|
ENSP00000502579.1:p.Glu595Val
|
|
ENST00000675517.1:c.2076A>T
|
|
|
ENST00000676076.1:c.2062A>T
|
|
|
ENST00000676260.1:c.2163A>T
|
|
|
ENST00000676316.1:c.2088A>T
|
|
|
ENST00000291825.11:c.*2406A>T
|
ENSP00000291825.6:n.*2406A>T
|
|
ENST00000324001.7:c.2201A>T
|
ENSP00000326018.6:p.Glu734Val
|
|
NM_020956.2:c.*2406A>T , LRG_265t1:c.*2406A>T
|
NP_066007.1:n.*2406A>T
|
|
NM_181882.2:c.2201A>T , LRG_265t2:c.2201A>T
|
NP_870998.2:p.Glu734Val
|
|
XM_011527171.1:c.2201A>T
|
XP_011525473.1:p.Glu734Val
|
|
XM_011527171.2:c.2201A>T
|
XP_011525473.1:p.Glu734Val
|
|
XM_017027046.1:c.2099A>T
|
XP_016882535.1:p.Glu700Val
|
|
XM_017027047.1:c.2099A>T
|
XP_016882536.1:p.Glu700Val
|
|
NM_181882.3:c.2201A>T
MANE Select
|
NP_870998.2:p.Glu734Val
|
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