ENST00000697571.1:c.2452C>A
(PALD1)
|
ENSP00000513342.1:p.Pro818Thr
|
|
ENST00000697572.1:c.2250+34402C>A
(PALD1)
|
ENSP00000513343.1:n.2250+34402C>A
|
|
ENST00000697573.1:c.2296C>A
(PALD1)
|
ENSP00000513344.1:p.Pro766Thr
|
|
ENST00000697577.1:n.2756C>A
(PALD1)
|
|
|
ENST00000697578.1:n.2600C>A
(PALD1)
|
|
|
ENST00000441259.2:c.800G>T
(PRF1)
MANE Select
|
ENSP00000398568.1:p.Gly267Val
|
|
ENST00000638674.1:c.540-1080G>T
(PRF1)
|
ENSP00000492048.1:n.540-1080G>T
|
|
ENST00000639390.1:n.98-1080G>T
(PRF1)
|
|
|
ENST00000373209.2:c.800G>T
(PRF1)
|
ENSP00000362305.1:p.Gly267Val
|
|
ENST00000441259.1:c.800G>T
(PRF1)
|
ENSP00000398568.1:p.Gly267Val
|
|
NM_001083116.1:c.800G>T , LRG_94t1:c.800G>T
(PRF1)
|
NP_001076585.1:p.Gly267Val
|
|
NM_005041.4:c.800G>T
(PRF1)
|
NP_005032.2:p.Gly267Val
|
|
NM_001083116.2:c.800G>T
(PRF1)
|
NP_001076585.1:p.Gly267Val
|
|
NM_005041.5:c.800G>T
(PRF1)
|
NP_005032.2:p.Gly267Val
|
|
NM_001083116.3:c.800G>T
(PRF1)
MANE Select
|
NP_001076585.1:p.Gly267Val
|
|
NM_005041.6:c.800G>T
(PRF1)
|
NP_005032.2:p.Gly267Val
|
|