ENST00000335670.11:c.166+191319A>T
MANE Select
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ENSP00000335087.6:n.166+191319A>T
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ENST00000335670.10:c.166+191319A>T
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ENSP00000335087.6:n.166+191319A>T
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ENST00000551975.5:c.81+191319A>T
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ENST00000557822.5:n.191+191319A>T
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ENST00000559145.1:n.173+191319A>T
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ENST00000561093.1:n.179+191319A>T
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NM_134261.2:c.166+191319A>T
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NP_599023.1:n.166+191319A>T
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XM_011521878.1:c.-328+191319A>T
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XP_011520180.1:n.-328+191319A>T
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XM_011521878.2:c.-328+191319A>T
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XP_011520180.1:n.-328+191319A>T
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XR_001751773.2:n.2391A>T
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XR_001751776.2:n.1088+1303A>T
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XR_001751777.2:n.967-2808A>T
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XR_002957755.1:n.7416A>T
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XR_002957756.1:n.4367A>T
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XR_002957757.1:n.7416A>T
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XR_002957758.1:n.7416A>T
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XR_002957759.1:n.7416A>T
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XR_002957760.1:n.11013A>T
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XR_002957761.1:n.7416A>T
|
|
|
NM_134261.3:c.166+191319A>T
MANE Select
|
NP_599023.1:n.166+191319A>T
|
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