ENST00000349184.9:c.546+759G>A
|
ENSP00000296979.4:n.546+759G>A
|
|
ENST00000296980.7:c.642+759G>A
MANE Select
|
ENSP00000296980.2:n.642+759G>A
|
|
ENST00000296980.6:c.642+759G>A
|
ENSP00000296980.2:n.642+759G>A
|
|
ENST00000339602.3:c.377-1190G>A
|
ENSP00000340920.3:n.377-1190G>A
|
|
ENST00000349184.8:c.546+759G>A
|
ENSP00000296979.4:n.546+759G>A
|
|
NM_052962.2:c.642+759G>A
|
NP_443194.1:n.642+759G>A
|
|
NM_181309.1:c.546+759G>A
|
NP_851826.1:n.546+759G>A
|
|
NM_181310.1:c.377-1190G>A
|
NP_851827.1:n.377-1190G>A
|
|
NM_052962.3:c.642+759G>A
MANE Select
|
NP_443194.1:n.642+759G>A
|
|
NM_181309.2:c.546+759G>A
|
NP_851826.1:n.546+759G>A
|
|
NM_181310.2:c.377-1190G>A
|
NP_851827.1:n.377-1190G>A
|
|