ENST00000697571.1:c.2453C>A
(PALD1)
|
ENSP00000513342.1:p.Pro818His
|
|
ENST00000697572.1:c.2250+34403C>A
(PALD1)
|
ENSP00000513343.1:n.2250+34403C>A
|
|
ENST00000697573.1:c.2297C>A
(PALD1)
|
ENSP00000513344.1:p.Pro766His
|
|
ENST00000697577.1:n.2757C>A
(PALD1)
|
|
|
ENST00000697578.1:n.2601C>A
(PALD1)
|
|
|
ENST00000441259.2:c.799G>T
(PRF1)
MANE Select
|
ENSP00000398568.1:p.Gly267Cys
|
|
ENST00000638674.1:c.540-1081G>T
(PRF1)
|
ENSP00000492048.1:n.540-1081G>T
|
|
ENST00000639390.1:n.98-1081G>T
(PRF1)
|
|
|
ENST00000373209.2:c.799G>T
(PRF1)
|
ENSP00000362305.1:p.Gly267Cys
|
|
ENST00000441259.1:c.799G>T
(PRF1)
|
ENSP00000398568.1:p.Gly267Cys
|
|
NM_001083116.1:c.799G>T , LRG_94t1:c.799G>T
(PRF1)
|
NP_001076585.1:p.Gly267Cys
|
|
NM_005041.4:c.799G>T
(PRF1)
|
NP_005032.2:p.Gly267Cys
|
|
NM_001083116.2:c.799G>T
(PRF1)
|
NP_001076585.1:p.Gly267Cys
|
|
NM_005041.5:c.799G>T
(PRF1)
|
NP_005032.2:p.Gly267Cys
|
|
NM_001083116.3:c.799G>T
(PRF1)
MANE Select
|
NP_001076585.1:p.Gly267Cys
|
|
NM_005041.6:c.799G>T
(PRF1)
|
NP_005032.2:p.Gly267Cys
|
|