ENST00000295897.9:c.482+183T>C
MANE Select
|
ENSP00000295897.4:n.482+183T>C
|
|
ENST00000295897.8:c.482+183T>C
|
ENSP00000295897.4:n.482+183T>C
|
|
ENST00000401494.7:c.138-367T>C
|
ENSP00000384695.3:n.138-367T>C
|
|
ENST00000415165.6:c.138-3008T>C
|
ENSP00000401820.2:n.138-3008T>C
|
|
ENST00000441319.5:c.488+183T>C
|
ENSP00000392541.1:n.488+183T>C
|
|
ENST00000476441.6:c.80-367T>C
|
ENSP00000423727.1:n.80-367T>C
|
|
ENST00000503124.5:c.33-367T>C
|
ENSP00000421027.1:n.33-367T>C
|
|
ENST00000505649.5:n.168+183T>C
|
|
|
ENST00000509063.5:c.482+183T>C
|
ENSP00000422784.1:n.482+183T>C
|
|
ENST00000514786.1:n.451+183T>C
|
|
|
ENST00000621085.4:c.482+183T>C
|
ENSP00000483421.1:n.482+183T>C
|
|
ENST00000621628.4:c.483-85T>C
|
ENSP00000480485.1:n.483-85T>C
|
|
NM_000477.5:c.482+183T>C
|
NP_000468.1:n.482+183T>C
|
|
NM_000477.6:c.482+183T>C
|
NP_000468.1:n.482+183T>C
|
|
NM_000477.7:c.482+183T>C
MANE Select
|
NP_000468.1:n.482+183T>C
|
|