ENST00000644269.2:c.1264-129G>T
MANE Select
|
ENSP00000494017.1:n.1264-129G>T
|
|
ENST00000265715.7:c.1264-129G>T
|
ENSP00000265715.3:n.1264-129G>T
|
|
ENST00000460748.1:n.367-129G>T
|
|
|
ENST00000477350.5:n.189-347G>T
|
|
|
ENST00000480841.5:n.113-129G>T
|
|
|
ENST00000497446.5:n.279-129G>T
|
|
|
NM_000441.1:c.1264-129G>T
|
NP_000432.1:n.1264-129G>T
|
|
XM_005250425.1:c.1264-129G>T
|
XP_005250482.1:n.1264-129G>T
|
|
XM_006716025.2:c.*714G>T
|
XP_006716088.1:n.*714G>T
|
|
XM_005250425.2:c.1264-129G>T
|
XP_005250482.1:n.1264-129G>T
|
|
XM_006716025.3:c.*714G>T
|
XP_006716088.1:n.*714G>T
|
|
XM_017012318.1:c.1264-347G>T
|
XP_016867807.1:n.1264-347G>T
|
|
NM_000441.2:c.1264-129G>T
MANE Select
|
NP_000432.1:n.1264-129G>T
|
|