ENST00000265403.12:c.718+21T>A
MANE Select
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ENSP00000265403.7:n.718+21T>A
|
|
ENST00000265403.11:c.718+21T>A
|
ENSP00000265403.7:n.718+21T>A
|
|
ENST00000458688.2:c.466+273T>A
|
ENSP00000413420.2:n.466+273T>A
|
|
NM_001075.5:c.718+21T>A
|
NP_001066.1:n.718+21T>A
|
|
NM_001144767.2:c.466+273T>A
|
NP_001138239.1:n.466+273T>A
|
|
NM_001290091.1:c.-27+586T>A
|
NP_001277020.1:n.-27+586T>A
|
|
XM_017008585.2:c.718+21T>A
|
XP_016864074.1:n.718+21T>A
|
|
NM_001075.6:c.718+21T>A
MANE Select
|
NP_001066.1:n.718+21T>A
|
|
NM_001144767.3:c.466+273T>A
|
NP_001138239.1:n.466+273T>A
|
|
NM_001290091.2:c.-27+586T>A
|
NP_001277020.1:n.-27+586T>A
|
|