|
NM_001080.3:c.727-3298G>A
MANE Select
|
NP_001071.1:n.727-3298G>A
|
|
ENST00000357578.8:c.727-3298G>A
MANE Select
|
ENSP00000350191.3:n.727-3298G>A
|
|
NM_001368954.1:c.726+6884G>A
|
NP_001355883.1:n.726+6884G>A
|
|
NM_170740.1:c.765+1G>A
|
NP_733936.1:n.765+1G>A
|
|
ENST00000348925.2:c.765+1G>A
|
ENSP00000314649.3:n.765+1G>A
|
|
ENST00000357578.7:c.727-3298G>A
|
ENSP00000350191.3:n.727-3298G>A
|
|
ENST00000491546.5:c.643-3298G>A
|
ENSP00000417687.1:n.643-3298G>A
|
|
ENST00000672352.1:c.489+6884G>A
|
ENSP00000500876.1:n.489+6884G>A
|
|
ENST00000672557.1:c.645-3298G>A
|
|
|
ENST00000672619.1:n.87-3298G>A
|
|
|
ENST00000672652.1:c.648-3256G>A
|
|
|
ENST00000675422.1:n.1487-3298G>A
|
|