ENST00000367618.8:c.2388+7249A>C
MANE Select
|
ENSP00000356590.3:n.2388+7249A>C
|
|
ENST00000367618.7:c.2388+7249A>C
|
ENSP00000356590.3:n.2388+7249A>C
|
|
ENST00000434088.1:c.2190+7249A>C
|
ENSP00000391716.1:n.2190+7249A>C
|
|
ENST00000457238.6:c.*367+7249A>C
|
ENSP00000416712.3:n.*367+7249A>C
|
|
ENST00000484883.1:n.132+7249A>C
|
|
|
ENST00000511157.5:c.*564-6633A>C
|
ENSP00000424373.1:n.*564-6633A>C
|
|
ENST00000617277.4:c.*563+7249A>C
|
ENSP00000482167.1:n.*563+7249A>C
|
|
NM_144696.5:c.2388+7249A>C
|
NP_653297.3:n.2388+7249A>C
|
|
NR_073544.1:n.2415-6633A>C
|
|
|
XM_011509165.1:c.2388+7249A>C
|
XP_011507467.1:n.2388+7249A>C
|
|
XM_011509166.1:c.2388+7249A>C
|
XP_011507468.1:n.2388+7249A>C
|
|
XM_011509167.1:c.2388+7249A>C
|
XP_011507469.1:n.2388+7249A>C
|
|
XM_011509168.1:c.2388+7249A>C
|
XP_011507470.1:n.2388+7249A>C
|
|
XM_011509169.1:c.2325+7249A>C
|
XP_011507471.1:n.2325+7249A>C
|
|
XM_011509170.1:c.2388+7249A>C
|
XP_011507472.1:n.2388+7249A>C
|
|
XM_011509171.1:c.2262+7249A>C
|
XP_011507473.1:n.2262+7249A>C
|
|
XM_011509172.1:c.2262+7249A>C
|
XP_011507474.1:n.2262+7249A>C
|
|
XM_011509173.1:c.2262+7249A>C
|
XP_011507475.1:n.2262+7249A>C
|
|
XM_011509174.1:c.2388+7249A>C
|
XP_011507476.1:n.2388+7249A>C
|
|
XM_011509175.1:c.2388+7249A>C
|
XP_011507477.1:n.2388+7249A>C
|
|
XM_011509176.1:c.2092-9096A>C
|
XP_011507478.1:n.2092-9096A>C
|
|
XM_011509177.1:c.2388+7249A>C
|
XP_011507479.1:n.2388+7249A>C
|
|
XM_011509179.1:c.1752+7249A>C
|
XP_011507481.1:n.1752+7249A>C
|
|
XM_011509180.1:c.2389-6633A>C
|
XP_011507482.1:n.2389-6633A>C
|
|
XM_011509181.1:c.1311+7249A>C
|
XP_011507483.1:n.1311+7249A>C
|
|
XR_921741.1:n.2755-4592A>C
|
|
|
XR_921742.1:n.2755-4592A>C
|
|
|
XM_011509166.3:c.2388+7249A>C
|
XP_011507468.1:n.2388+7249A>C
|
|
XM_011509167.3:c.2388+7249A>C
|
XP_011507469.1:n.2388+7249A>C
|
|
XM_011509179.2:c.1752+7249A>C
|
XP_011507481.1:n.1752+7249A>C
|
|
XM_011509181.2:c.1311+7249A>C
|
XP_011507483.1:n.1311+7249A>C
|
|
XM_017000257.2:c.1647+7249A>C
|
XP_016855746.1:n.1647+7249A>C
|
|
XM_017000258.2:c.1509+7249A>C
|
XP_016855747.1:n.1509+7249A>C
|
|
XM_024453104.1:c.2262+7249A>C
|
XP_024308872.1:n.2262+7249A>C
|
|
XM_024453107.1:c.2262+7249A>C
|
XP_024308875.1:n.2262+7249A>C
|
|
XR_921742.2:n.2755-4592A>C
|
|
|
NM_144696.6:c.2388+7249A>C
MANE Select
|
NP_653297.3:n.2388+7249A>C
|
|
NR_073544.2:n.2343-6633A>C
|
|
|