ENST00000396705.10:c.543+129C>T
MANE Select
|
ENSP00000379933.4:n.543+129C>T
|
|
ENST00000229270.8:c.654+129C>T
|
ENSP00000229270.4:n.654+129C>T
|
|
ENST00000396705.9:c.543+129C>T
|
ENSP00000379933.4:n.543+129C>T
|
|
ENST00000482209.1:n.226+129C>T
|
|
|
ENST00000488464.6:c.297+129C>T
|
ENSP00000475620.1:n.297+129C>T
|
|
ENST00000493987.5:c.297+129C>T
|
ENSP00000475364.1:n.297+129C>T
|
|
ENST00000535434.5:c.297+129C>T
|
ENSP00000443599.1:n.297+129C>T
|
|
ENST00000613953.4:c.654+129C>T
|
ENSP00000484435.1:n.654+129C>T
|
|
NM_000365.5:c.543+129C>T
|
NP_000356.1:n.543+129C>T
|
|
NM_001159287.1:c.654+129C>T
|
NP_001152759.1:n.654+129C>T
|
|
NM_001258026.1:c.297+129C>T
|
NP_001244955.1:n.297+129C>T
|
|
XR_002957378.1:n.1405C>T
|
|
|
NM_000365.6:c.543+129C>T
MANE Select
|
NP_000356.1:n.543+129C>T
|
|
NM_001258026.2:c.297+129C>T
|
NP_001244955.1:n.297+129C>T
|
|