ENST00000544665.9:c.238+30G>A
MANE Select
|
ENSP00000441691.3:n.238+30G>A
|
|
ENST00000648685.1:c.238+30G>A
|
ENSP00000496959.1:n.238+30G>A
|
|
ENST00000287497.12:c.238+30G>A
|
ENSP00000287497.8:n.238+30G>A
|
|
ENST00000544665.7:c.238+30G>A
|
ENSP00000441691.2:n.238+30G>A
|
|
NM_000632.3:c.238+30G>A
|
NP_000623.2:n.238+30G>A
|
|
NM_001145808.1:c.238+30G>A
|
NP_001139280.1:n.238+30G>A
|
|
XM_006721045.1:c.238+30G>A
|
XP_006721108.1:n.238+30G>A
|
|
XM_011545850.1:c.23+30G>A
|
XP_011544152.1:n.23+30G>A
|
|
XM_011545851.1:c.238+30G>A
|
XP_011544153.1:n.238+30G>A
|
|
XR_950796.1:n.328+30G>A
|
|
|
XM_011545850.2:c.23+30G>A
|
XP_011544152.1:n.23+30G>A
|
|
XM_011545851.2:c.238+30G>A
|
XP_011544153.1:n.238+30G>A
|
|
XM_017023216.1:c.238+30G>A
|
XP_016878705.1:n.238+30G>A
|
|
NM_000632.4:c.238+30G>A
MANE Select
|
NP_000623.2:n.238+30G>A
|
|
NM_001145808.2:c.238+30G>A
|
NP_001139280.1:n.238+30G>A
|
|