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MANE Plus Clinical
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ENST00000550418.6:c.28-108962T>C
MANE Select
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ENSP00000450031.1:n.28-108962T>C
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NM_145893.2:c.87+76097T>C
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XP_011520850.1:n.87+76097T>C
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XP_016878831.1:n.28-108962T>C
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XP_024306072.1:n.136-108962T>C
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XP_024306073.1:n.136-108962T>C
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XP_024306074.1:n.87+76097T>C
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XP_024306075.1:n.28-108962T>C
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XP_024306076.1:n.102+104700T>C
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XM_024450309.1:c.157-108962T>C
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XP_024306077.1:n.157-108962T>C
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XM_024450310.1:c.157-108962T>C
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XP_024306078.1:n.157-108962T>C
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XM_024450311.1:c.136-108962T>C
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XP_024306079.1:n.136-108962T>C
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XM_024450312.1:c.136-108962T>C
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XP_024306080.1:n.136-108962T>C
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XM_024450313.1:c.136-108962T>C
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XP_024306081.1:n.136-108962T>C
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XM_024450314.1:c.157-108962T>C
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XP_024306082.1:n.157-108962T>C
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XM_024450316.1:c.28-108962T>C
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XP_024306084.1:n.28-108962T>C
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NM_001142333.2:c.28-108962T>C
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NP_001135805.1:n.28-108962T>C
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NM_001364800.2:c.28-108962T>C
|
NP_001351729.1:n.28-108962T>C
|
|
NM_018723.4:c.28-108962T>C
MANE Select
|
NP_061193.2:n.28-108962T>C
|
|
NM_145891.3:c.87+76097T>C
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NP_665898.1:n.87+76097T>C
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NM_145892.3:c.87+76097T>C
|
NP_665899.1:n.87+76097T>C
|
|
NM_145893.3:c.87+76097T>C
MANE Plus Clinical
|
NP_665900.1:n.87+76097T>C
|
|
NM_001142334.2:c.28-108962T>C
|
NP_001135806.1:n.28-108962T>C
|
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