ENST00000382103.7:c.389-140G>A
MANE Select
|
ENSP00000371535.2:n.389-140G>A
|
|
ENST00000680581.1:c.389-140G>A
|
ENSP00000506483.1:n.389-140G>A
|
|
ENST00000680824.1:n.1605-140G>A
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|
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ENST00000681071.1:n.681-140G>A
|
|
|
ENST00000681166.1:n.1436-140G>A
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|
|
ENST00000681341.1:n.1530-140G>A
|
|
|
ENST00000681640.1:n.483-140G>A
|
|
|
ENST00000681948.1:c.644-140G>A
|
ENSP00000505991.1:n.644-140G>A
|
|
ENST00000358971.7:c.*187-140G>A
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ENSP00000351857.3:n.*187-140G>A
|
|
ENST00000382103.6:c.389-140G>A
|
ENSP00000371535.2:n.389-140G>A
|
|
ENST00000514585.5:c.*90-140G>A
|
ENSP00000421880.1:n.*90-140G>A
|
|
NM_016955.3:c.389-140G>A
|
NP_058651.3:n.389-140G>A
|
|
XM_005248168.2:c.152-140G>A
|
XP_005248225.1:n.152-140G>A
|
|
XM_006713965.2:c.209-140G>A
|
XP_006714028.1:n.209-140G>A
|
|
XM_011513846.1:c.386-140G>A
|
XP_011512148.1:n.386-140G>A
|
|
XM_011513847.1:c.356-140G>A
|
XP_011512149.1:n.356-140G>A
|
|
XM_011513848.1:c.209-140G>A
|
XP_011512150.1:n.209-140G>A
|
|
XM_011513846.2:c.386-140G>A
|
XP_011512148.1:n.386-140G>A
|
|
XM_011513847.2:c.356-140G>A
|
XP_011512149.1:n.356-140G>A
|
|
XM_017008277.1:c.644-140G>A
|
XP_016863766.1:n.644-140G>A
|
|
XM_017008278.1:c.-35-140G>A
|
XP_016863767.1:n.-35-140G>A
|
|
NM_016955.4:c.389-140G>A
MANE Select
|
NP_058651.3:n.389-140G>A
|
|