ENST00000310546.3:c.694+13608T>A
MANE Select
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ENSP00000311609.2:n.694+13608T>A
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ENST00000310546.2:c.694+13608T>A
|
ENSP00000311609.2:n.694+13608T>A
|
|
ENST00000507895.1:n.255T>A
|
|
|
ENST00000508126.1:c.161+13608T>A
|
|
|
NM_080862.2:c.694+13608T>A
|
NP_543138.1:n.694+13608T>A
|
|
XM_011513313.1:c.694+13608T>A
|
XP_011511615.1:n.694+13608T>A
|
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XR_924215.1:n.1545T>A
|
|
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XR_924216.1:n.1545T>A
|
|
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XM_017007509.2:c.*109T>A
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XP_016862998.1:n.*109T>A
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|
XR_924215.3:n.1026T>A
|
|
|
XR_924216.3:n.1026T>A
|
|
|
NM_080862.3:c.694+13608T>A
MANE Select
|
NP_543138.1:n.694+13608T>A
|
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