ENST00000274695.8:c.517+8298A>G
MANE Select
|
ENSP00000274695.4:n.517+8298A>G
|
|
ENST00000378610.1:c.517+8298A>G
|
ENSP00000367873.1:n.517+8298A>G
|
|
NM_017774.3:c.517+8298A>G
MANE Select
|
NP_060244.2:n.517+8298A>G
|
|
XM_006715128.2:c.517+8298A>G
|
XP_006715191.1:n.517+8298A>G
|
|
XM_011514718.1:c.517+8298A>G
|
XP_011513020.1:n.517+8298A>G
|
|
XM_011514719.1:c.517+8298A>G
|
XP_011513021.1:n.517+8298A>G
|
|
XR_926265.1:n.684+8298A>G
|
|
|
XR_926266.1:n.797+8298A>G
|
|
|
XR_926267.1:n.684+8298A>G
|
|
|
XM_011514719.2:c.517+8298A>G
|
XP_011513021.1:n.517+8298A>G
|
|
XM_017010986.1:c.517+8298A>G
|
XP_016866475.1:n.517+8298A>G
|
|
XM_017010987.1:c.-238+8298A>G
|
XP_016866476.1:n.-238+8298A>G
|
|
XM_024446481.1:c.517+8298A>G
|
XP_024302249.1:n.517+8298A>G
|
|
XR_001743495.2:n.689+8298A>G
|
|
|
XR_001743496.2:n.1084+8298A>G
|
|
|
XR_001743500.1:n.684+8298A>G
|
|
|
XR_001743501.1:n.684+8298A>G
|
|
|
XR_926265.2:n.684+8298A>G
|
|
|
XR_926266.2:n.797+8298A>G
|
|
|
XR_926267.2:n.684+8298A>G
|
|
|