ENST00000243578.8:c.*113C>A
(B9D2)
MANE Select
|
ENSP00000243578.2:n.*113C>A
|
|
ENST00000675972.1:c.*113C>A
(B9D2)
|
ENSP00000501911.1:n.*113C>A
|
|
ENST00000243578.7:c.*113C>A
(B9D2)
|
ENSP00000243578.2:n.*113C>A
|
|
ENST00000539627.5:c.-30+3385G>T
(TMEM91)
|
ENSP00000441900.1:n.-30+3385G>T
|
|
ENST00000604123.5:c.142+272G>T
(TMEM91)
|
ENSP00000474871.1:n.142+272G>T
|
|
ENST00000604424.1:n.350+3385G>T
|
|
|
NM_030578.3:c.*113C>A
(B9D2)
|
NP_085055.2:n.*113C>A
|
|
XM_006723405.1:c.*113C>A
(B9D2)
|
XP_006723468.1:n.*113C>A
|
|
XM_011527349.1:c.*113C>A
(B9D2)
|
XP_011525651.1:n.*113C>A
|
|
XM_011527350.1:c.*113C>A
(B9D2)
|
XP_011525652.1:n.*113C>A
|
|
XM_011527349.2:c.*113C>A
(B9D2)
|
XP_011525651.1:n.*113C>A
|
|
XM_011527350.2:c.*113C>A
(B9D2)
|
XP_011525652.1:n.*113C>A
|
|
NM_030578.4:c.*113C>A
(B9D2)
MANE Select
|
NP_085055.2:n.*113C>A
|
|