ENST00000299665.3:c.28+445T>A
MANE Select
|
ENSP00000299665.2:n.28+445T>A
|
|
ENST00000299665.2:c.28+445T>A
|
ENSP00000299665.2:n.28+445T>A
|
|
ENST00000382064.6:c.28+445T>A
|
ENSP00000371496.2:n.28+445T>A
|
|
NM_080387.4:c.28+445T>A
|
NP_525126.2:n.28+445T>A
|
|
XM_011520632.1:c.28+445T>A
|
XP_011518934.1:n.28+445T>A
|
|
XM_011520633.1:c.28+445T>A
|
XP_011518935.1:n.28+445T>A
|
|
XM_011520632.2:c.28+445T>A
|
XP_011518934.1:n.28+445T>A
|
|
XM_011520633.2:c.28+445T>A
|
XP_011518935.1:n.28+445T>A
|
|
NM_080387.5:c.28+445T>A
MANE Select
|
NP_525126.2:n.28+445T>A
|
|