ENST00000298912.9:c.82+21589T>C
MANE Select
|
ENSP00000298912.3:n.82+21589T>C
|
|
ENST00000298912.8:c.82+21589T>C
|
ENSP00000298912.3:n.82+21589T>C
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|
ENST00000553733.1:c.82+21589T>C
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ENSP00000451189.1:n.82+21589T>C
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|
ENST00000555615.1:c.-123+9392T>C
|
ENSP00000452525.1:n.-123+9392T>C
|
|
NM_024734.3:c.82+21589T>C
|
NP_079010.2:n.82+21589T>C
|
|
XM_011537158.1:c.82+21589T>C
|
XP_011535460.1:n.82+21589T>C
|
|
XM_011537159.1:c.82+21589T>C
|
XP_011535461.1:n.82+21589T>C
|
|
XR_245721.2:n.194+21589T>C
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|
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XR_429330.2:n.194+21589T>C
|
|
|
XR_429332.2:n.194+21589T>C
|
|
|
XM_011537159.2:c.82+21589T>C
|
XP_011535461.1:n.82+21589T>C
|
|
XM_017021646.1:c.22+21117T>C
|
XP_016877135.1:n.22+21117T>C
|
|
XM_017021647.1:c.82+21589T>C
|
XP_016877136.1:n.82+21589T>C
|
|
XR_001750558.1:n.194+21589T>C
|
|
|
NM_024734.4:c.82+21589T>C
MANE Select
|
NP_079010.2:n.82+21589T>C
|
|