ENST00000225609.10:c.494+17G>A
MANE Select
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ENSP00000225609.5:n.494+17G>A
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ENST00000225609.9:c.494+17G>A
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ENSP00000225609.5:n.494+17G>A
|
|
ENST00000395844.8:c.494+17G>A
|
ENSP00000379185.3:n.494+17G>A
|
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ENST00000477745.5:n.492+17G>A
|
|
|
ENST00000498772.6:n.511+17G>A
|
|
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ENST00000580201.1:n.506+17G>A
|
|
|
ENST00000581006.5:c.426+13653G>A
|
ENSP00000462432.1:n.426+13653G>A
|
|
ENST00000584797.5:c.494+17G>A
|
ENSP00000463540.1:n.494+17G>A
|
|
ENST00000585034.5:c.*88+17G>A
|
ENSP00000464424.1:n.*88+17G>A
|
|
ENST00000596678.2:c.68+17G>A
|
ENSP00000470064.2:n.68+17G>A
|
|
NM_004278.3:c.494+17G>A
|
NP_004269.1:n.494+17G>A
|
|
XM_011524080.1:c.494+17G>A
|
XP_011522382.1:n.494+17G>A
|
|
XR_243571.2:n.512+17G>A
|
|
|
XR_429826.2:n.512+17G>A
|
|
|
XM_011524080.2:c.494+17G>A
|
XP_011522382.1:n.494+17G>A
|
|
XM_017025349.1:c.494+17G>A
|
XP_016880838.1:n.494+17G>A
|
|
XM_017025350.1:c.494+17G>A
|
XP_016880839.1:n.494+17G>A
|
|
XM_017025351.1:c.494+17G>A
|
XP_016880840.1:n.494+17G>A
|
|
XM_017025352.1:c.494+17G>A
|
XP_016880841.1:n.494+17G>A
|
|
XM_017025353.1:c.494+17G>A
|
XP_016880842.1:n.494+17G>A
|
|
XM_017025354.1:c.494+17G>A
|
XP_016880843.1:n.494+17G>A
|
|
XM_017025355.1:c.494+17G>A
|
XP_016880844.1:n.494+17G>A
|
|
XM_017025356.1:c.494+17G>A
|
XP_016880845.1:n.494+17G>A
|
|
NM_004278.4:c.494+17G>A
MANE Select
|
NP_004269.1:n.494+17G>A
|
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