ENST00000296589.9:c.385+2T>A
MANE Select
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ENSP00000296589.4:n.385+2T>A
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|
ENST00000296589.8:c.385+2T>A
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ENSP00000296589.4:n.385+2T>A
|
|
ENST00000382102.7:c.385+2T>A
|
ENSP00000371534.3:n.385+2T>A
|
|
ENST00000505056.1:n.364+2T>A
|
|
|
ENST00000509381.1:c.385+2T>A
|
ENSP00000421100.1:n.385+2T>A
|
|
ENST00000510600.1:c.37+2T>A
|
ENSP00000424010.1:n.37+2T>A
|
|
NM_001012509.3:c.385+2T>A
|
NP_001012527.1:n.385+2T>A
|
|
NM_001297417.2:c.385+2T>A
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NP_001284346.2:n.385+2T>A
|
|
NM_016180.4:c.385+2T>A
|
NP_057264.3:n.385+2T>A
|
|
XM_011514052.1:c.385+2T>A
|
XP_011512354.1:n.385+2T>A
|
|
XR_925620.1:n.946+2T>A
|
|
|
NM_016180.5:c.385+2T>A
MANE Select
|
NP_057264.4:n.385+2T>A
|
|
NM_001012509.4:c.385+2T>A
|
NP_001012527.2:n.385+2T>A
|
|
NM_001297417.3:c.385+2T>A
|
NP_001284346.2:n.385+2T>A
|
|
NM_001297417.4:c.385+2T>A
|
NP_001284346.2:n.385+2T>A
|
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