|
NM_020939.2:c.1563+416T>G
MANE Select
|
NP_065990.1:n.1563+416T>G
|
|
ENST00000244751.7:c.1563+416T>G
MANE Select
|
ENSP00000244751.2:n.1563+416T>G
|
|
NM_001314018.1:c.687+416T>G
|
NP_001300947.1:n.687+416T>G
|
|
NM_001314018.2:c.687+416T>G
|
NP_001300947.1:n.687+416T>G
|
|
NM_001314019.1:c.513+416T>G
|
NP_001300948.1:n.513+416T>G
|
|
NM_001314019.2:c.513+416T>G
|
NP_001300948.1:n.513+416T>G
|
|
NM_001314020.1:c.513+416T>G
|
NP_001300949.1:n.513+416T>G
|
|
NM_001314020.2:c.513+416T>G
|
NP_001300949.1:n.513+416T>G
|
|
NM_001376888.1:c.513+416T>G
|
NP_001363817.1:n.513+416T>G
|
|
NM_001376889.1:c.1614+416T>G
|
NP_001363818.1:n.1614+416T>G
|
|
NM_001376890.1:c.687+416T>G
|
NP_001363819.1:n.687+416T>G
|
|
NM_001376891.1:c.687+416T>G
|
NP_001363820.1:n.687+416T>G
|
|
NM_001376892.1:c.*17T>G
|
NP_001363821.1:n.*17T>G
|
|
NM_001376893.1:c.*17T>G
|
NP_001363822.1:n.*17T>G
|
|
NM_001376894.1:c.833+416T>G
|
NP_001363823.1:n.833+416T>G
|
|
NM_001376895.1:c.*17T>G
|
NP_001363824.1:n.*17T>G
|
|
NM_020939.1:c.1563+416T>G
|
NP_065990.1:n.1563+416T>G
|
|
ENST00000244751.6:c.1563+416T>G
|
ENSP00000244751.2:n.1563+416T>G
|
|
ENST00000393189.2:c.687+416T>G
|
ENSP00000376885.2:n.687+416T>G
|
|
ENST00000459703.5:n.846+416T>G
|
|
|
ENST00000493411.2:n.743+416T>G
|
|
|
ENST00000633136.2:c.1614+416T>G
|
ENSP00000487872.2:n.1614+416T>G
|
|
XM_005249247.1:c.1614+416T>G
|
XP_005249304.1:n.1614+416T>G
|
|
XM_005249247.2:c.1614+416T>G
|
XP_005249304.1:n.1614+416T>G
|
|
XM_005249249.2:c.1615-36T>G
|
XP_005249306.1:n.1615-36T>G
|
|
XM_011514768.1:c.*17T>G
|
XP_011513070.1:n.*17T>G
|
|
XM_011514769.1:c.*17T>G
|
XP_011513071.1:n.*17T>G
|
|
XM_011514770.1:c.*17T>G
|
XP_011513072.1:n.*17T>G
|
|
XM_011514771.1:c.*17T>G
|
XP_011513073.1:n.*17T>G
|
|
XM_011514771.2:c.*17T>G
|
XP_011513073.1:n.*17T>G
|
|
XM_011514773.1:c.*17T>G
|
XP_011513075.1:n.*17T>G
|
|
XM_011514773.2:c.*17T>G
|
XP_011513075.1:n.*17T>G
|
|
XM_011514775.1:c.*17T>G
|
XP_011513077.1:n.*17T>G
|
|
XM_011514775.2:c.*17T>G
|
XP_011513077.1:n.*17T>G
|
|
XM_011514776.1:c.*17T>G
|
XP_011513078.1:n.*17T>G
|
|
XM_011514777.1:c.*17T>G
|
XP_011513079.1:n.*17T>G
|
|
XM_011514778.1:c.*17T>G
|
XP_011513080.1:n.*17T>G
|
|
XM_017011139.2:c.*17T>G
|
XP_016866628.1:n.*17T>G
|
|
XM_024446500.1:c.513+416T>G
|
XP_024302268.1:n.513+416T>G
|
|
XR_002956290.1:n.1753+416T>G
|
|
|
XR_002956291.1:n.1619+416T>G
|
|
