ENST00000547103.7:c.6263A>T
MANE Select
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ENSP00000447211.2:p.Glu2088Val
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ENST00000642294.1:c.203A>T
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ENSP00000493572.1:p.Glu68Val
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ENST00000646859.1:c.6128A>T
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ENSP00000496036.1:p.Glu2043Val
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ENST00000298820.7:c.1527+121A>T
|
|
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ENST00000458043.6:c.6236A>T
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ENSP00000400895.2:p.Glu2079Val
|
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ENST00000546620.5:n.519A>T
|
|
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ENST00000547103.5:c.6200A>T
|
ENSP00000447211.1:p.Glu2067Val
|
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ENST00000550182.2:c.287A>T
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ENSP00000449641.1:p.Glu96Val
|
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ENST00000551340.5:c.391A>T
|
|
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NM_173591.3:c.6236A>T
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NP_775862.3:p.Glu2079Val
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XM_005268802.2:c.6287A>T
|
XP_005268859.1:p.Glu2096Val
|
|
XM_011538191.1:c.6287A>T
|
XP_011536493.1:p.Glu2096Val
|
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XM_011538192.1:c.6134A>T
|
XP_011536494.1:p.Glu2045Val
|
|
XM_011538193.1:c.5921A>T
|
XP_011536495.1:p.Glu1974Val
|
|
XM_005268802.3:c.6287A>T
|
XP_005268859.1:p.Glu2096Val
|
|
XM_011538192.2:c.6134A>T
|
XP_011536494.1:p.Glu2045Val
|
|
NM_001368062.1:c.6101A>T
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NP_001354991.1:p.Glu2034Val
|
|
NM_001368062.3:c.6128A>T
|
NP_001354991.2:p.Glu2043Val
|
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NM_001378609.3:c.6263A>T
MANE Select
|
NP_001365538.2:p.Glu2088Val
|
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NM_001378610.3:c.6263A>T
|
NP_001365539.2:p.Glu2088Val
|
|
NM_173591.7:c.6263A>T
|
NP_775862.4:p.Glu2088Val
|
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