ENST00000243578.8:c.-7A>C
(B9D2)
MANE Select
|
ENSP00000243578.2:n.-7A>C
|
|
ENST00000243578.7:c.-7A>C
(B9D2)
|
ENSP00000243578.2:n.-7A>C
|
|
ENST00000539627.5:c.-30+12758T>G
(TMEM91)
|
ENSP00000441900.1:n.-30+12758T>G
|
|
ENST00000594416.1:c.-7A>C
(B9D2)
|
ENSP00000469666.1:n.-7A>C
|
|
ENST00000601597.1:n.133A>C
(B9D2)
|
|
|
ENST00000604123.5:c.142+9645T>G
(TMEM91)
|
ENSP00000474871.1:n.142+9645T>G
|
|
ENST00000604424.1:n.350+12758T>G
|
|
|
NM_030578.3:c.-7A>C
(B9D2)
|
NP_085055.2:n.-7A>C
|
|
XM_006723405.1:c.-7A>C
(B9D2)
|
XP_006723468.1:n.-7A>C
|
|
XM_011527350.1:c.-74A>C
(B9D2)
|
XP_011525652.1:n.-74A>C
|
|
XM_011527350.2:c.-74A>C
(B9D2)
|
XP_011525652.1:n.-74A>C
|
|
NM_030578.4:c.-7A>C
(B9D2)
MANE Select
|
NP_085055.2:n.-7A>C
|
|
NM_001369864.1:c.-422T>G
(TMEM91)
|
NP_001356793.1:n.-422T>G
|
|
NM_001098825.2:c.-165T>G
(TMEM91)
|
NP_001092295.1:n.-165T>G
|
|