ENST00000348931.9:c.889+42G>C
MANE Select
|
ENSP00000335384.5:n.889+42G>C
|
|
ENST00000348931.8:c.889+42G>C
|
ENSP00000335384.5:n.889+42G>C
|
|
ENST00000377940.3:c.823+42G>C
|
ENSP00000367174.3:n.823+42G>C
|
|
ENST00000583811.5:c.535+42G>C
|
ENSP00000462463.1:n.535+42G>C
|
|
ENST00000584588.5:c.670+42G>C
|
ENSP00000462067.1:n.670+42G>C
|
|
NM_198844.2:c.823+42G>C
|
NP_942141.2:n.823+42G>C
|
|
NM_199321.2:c.889+42G>C
|
NP_955353.1:n.889+42G>C
|
|
XR_002957959.1:n.1094+42G>C
|
|
|
NM_198844.3:c.823+42G>C
|
NP_942141.2:n.823+42G>C
|
|
NM_199321.3:c.889+42G>C
MANE Select
|
NP_955353.1:n.889+42G>C
|
|