ENST00000366425.4:c.10+126G>T
(GP1BB)
MANE Select
|
ENSP00000383382.2:n.10+126G>T
|
|
ENST00000366425.3:c.10+126G>T
(GP1BB)
|
ENSP00000383382.2:n.10+126G>T
|
|
ENST00000431044.5:c.*1095+126G>T
(SEPTIN5)
|
ENSP00000399685.1:n.*1095+126G>T
|
|
ENST00000455843.5:c.*1095+126G>T
(SEPTIN5)
|
ENSP00000391731.1:n.*1095+126G>T
|
|
ENST00000470814.1:n.1982+126G>T
(SEPTIN5)
|
|
|
NM_000407.4:c.10+126G>T , LRG_478t1:c.10+126G>T
(GP1BB)
|
NP_000398.1:n.10+126G>T
|
|
NR_037611.1:n.3750+126G>T
|
|
|
NR_037612.1:n.2254+126G>T
|
|
|
NM_000407.5:c.10+126G>T
(GP1BB)
MANE Select
|
NP_000398.1:n.10+126G>T
|
|