ENST00000243578.8:c.-5+5G>A
(B9D2)
MANE Select
|
ENSP00000243578.2:n.-5+5G>A
|
|
ENST00000243578.7:c.-5+5G>A
(B9D2)
|
ENSP00000243578.2:n.-5+5G>A
|
|
ENST00000539627.5:c.-30+12751C>T
(TMEM91)
|
ENSP00000441900.1:n.-30+12751C>T
|
|
ENST00000594416.1:c.-5+5G>A
(B9D2)
|
ENSP00000469666.1:n.-5+5G>A
|
|
ENST00000601597.1:n.135+5G>A
(B9D2)
|
|
|
ENST00000604123.5:c.142+9638C>T
(TMEM91)
|
ENSP00000474871.1:n.142+9638C>T
|
|
ENST00000604424.1:n.350+12751C>T
|
|
|
NM_030578.3:c.-5+5G>A
(B9D2)
|
NP_085055.2:n.-5+5G>A
|
|
XM_006723405.1:c.-5+5G>A
(B9D2)
|
XP_006723468.1:n.-5+5G>A
|
|
XM_011527350.1:c.-72+5G>A
(B9D2)
|
XP_011525652.1:n.-72+5G>A
|
|
XM_011527350.2:c.-72+5G>A
(B9D2)
|
XP_011525652.1:n.-72+5G>A
|
|
NM_030578.4:c.-5+5G>A
(B9D2)
MANE Select
|
NP_085055.2:n.-5+5G>A
|
|
NM_001369864.1:c.-429C>T
(TMEM91)
|
NP_001356793.1:n.-429C>T
|
|
NM_001098825.2:c.-172C>T
(TMEM91)
|
NP_001092295.1:n.-172C>T
|
|