ENST00000644269.2:c.1264-118G>A
MANE Select
|
ENSP00000494017.1:n.1264-118G>A
|
|
ENST00000265715.7:c.1264-118G>A
|
ENSP00000265715.3:n.1264-118G>A
|
|
ENST00000460748.1:n.367-118G>A
|
|
|
ENST00000477350.5:n.189-336G>A
|
|
|
ENST00000480841.5:n.113-118G>A
|
|
|
ENST00000497446.5:n.279-118G>A
|
|
|
NM_000441.1:c.1264-118G>A
|
NP_000432.1:n.1264-118G>A
|
|
XM_005250425.1:c.1264-118G>A
|
XP_005250482.1:n.1264-118G>A
|
|
XM_006716025.2:c.*725G>A
|
XP_006716088.1:n.*725G>A
|
|
XM_005250425.2:c.1264-118G>A
|
XP_005250482.1:n.1264-118G>A
|
|
XM_006716025.3:c.*725G>A
|
XP_006716088.1:n.*725G>A
|
|
XM_017012318.1:c.1264-336G>A
|
XP_016867807.1:n.1264-336G>A
|
|
NM_000441.2:c.1264-118G>A
MANE Select
|
NP_000432.1:n.1264-118G>A
|
|