ENST00000278483.8:c.539+138T>C
MANE Select
|
ENSP00000278483.3:n.539+138T>C
|
|
ENST00000278483.7:c.539+138T>C
|
ENSP00000278483.3:n.539+138T>C
|
|
ENST00000528004.5:c.*562T>C
|
ENSP00000433815.1:n.*562T>C
|
|
ENST00000529405.1:n.1214+138T>C
|
|
|
ENST00000530208.1:n.614+138T>C
|
|
|
ENST00000531485.5:n.507+138T>C
|
|
|
ENST00000533986.5:c.*92T>C
|
ENSP00000432699.1:n.*92T>C
|
|
ENST00000618164.1:c.341+138T>C
|
ENSP00000482151.1:n.341+138T>C
|
|
NM_016401.3:c.539+138T>C
|
NP_057485.2:n.539+138T>C
|
|
NR_024596.1:n.614+138T>C
|
|
|
NR_024597.1:n.539+138T>C
|
|
|
NR_024598.1:n.539+138T>C
|
|
|
XM_011545097.1:c.422+138T>C
|
XP_011543399.1:n.422+138T>C
|
|
XR_949963.1:n.762+138T>C
|
|
|
XR_950386.1:n.77-7926A>G
|
|
|
NM_001322404.1:c.479+138T>C
|
NP_001309333.1:n.479+138T>C
|
|
NM_001322407.1:c.422+138T>C
|
NP_001309336.1:n.422+138T>C
|
|
NM_001322409.1:c.422+138T>C
|
NP_001309338.1:n.422+138T>C
|
|
NR_136324.1:n.885+138T>C
|
|
|
XM_017017914.2:c.539+138T>C
|
XP_016873403.1:n.539+138T>C
|
|
XM_017017915.1:c.422+138T>C
|
XP_016873404.1:n.422+138T>C
|
|
XR_001747904.2:n.886T>C
|
|
|
XR_001748531.1:n.261-7926A>G
|
|
|
XR_949963.3:n.748+138T>C
|
|
|
NM_016401.4:c.539+138T>C
MANE Select
|
NP_057485.2:n.539+138T>C
|
|
NM_001322404.2:c.479+138T>C
|
NP_001309333.1:n.479+138T>C
|
|
NM_001322407.2:c.422+138T>C
|
NP_001309336.1:n.422+138T>C
|
|
NM_001322409.2:c.422+138T>C
|
NP_001309338.1:n.422+138T>C
|
|
NR_024597.2:n.510+138T>C
|
|
|
NR_024598.2:n.510+138T>C
|
|
|
NR_136324.2:n.872+138T>C
|
|
|