ENST00000221086.8:c.971+1302A>T
MANE Select
|
ENSP00000221086.3:n.971+1302A>T
|
|
ENST00000221086.7:c.971+1302A>T
|
ENSP00000221086.3:n.971+1302A>T
|
|
ENST00000526292.1:c.716+1302A>T
|
ENSP00000433239.1:n.716+1302A>T
|
|
ENST00000530200.1:c.*717+1302A>T
|
ENSP00000436046.1:n.*717+1302A>T
|
|
NM_015458.3:c.971+1302A>T
|
NP_056273.2:n.971+1302A>T
|
|
XM_011543830.1:c.650+1302A>T
|
XP_011542132.1:n.650+1302A>T
|
|
XM_011543831.1:c.383+1302A>T
|
XP_011542133.1:n.383+1302A>T
|
|
XM_011543830.3:c.650+1302A>T
|
XP_011542132.1:n.650+1302A>T
|
|
XM_011543831.2:c.383+1302A>T
|
XP_011542133.1:n.383+1302A>T
|
|
XM_017013753.2:c.971+1302A>T
|
XP_016869242.1:n.971+1302A>T
|
|
NM_015458.4:c.971+1302A>T
MANE Select
|
NP_056273.2:n.971+1302A>T
|
|