ENST00000700559.2:c.1556+11C>G
|
ENSP00000515065.2:n.1556+11C>G
|
|
ENST00000700563.2:c.1556+11C>G
|
ENSP00000515066.2:n.1556+11C>G
|
|
ENST00000700556.1:c.27+11C>G
|
|
|
ENST00000700559.1:c.771+11C>G
|
|
|
ENST00000700560.1:n.771+11C>G
|
|
|
ENST00000700561.1:n.897+11C>G
|
|
|
ENST00000700563.1:c.1510+11C>G
|
|
|
ENST00000700564.1:n.1560+11C>G
|
|
|
ENST00000700565.1:n.1420C>G
|
|
|
ENST00000070846.11:c.1688+11C>G
|
ENSP00000070846.6:n.1688+11C>G
|
|
ENST00000340811.9:c.1556+11C>G
MANE Select
|
ENSP00000342800.5:n.1556+11C>G
|
|
ENST00000070846.10:c.1688+11C>G
|
ENSP00000070846.6:n.1688+11C>G
|
|
ENST00000340811.8:c.1556+11C>G
|
ENSP00000342800.4:n.1556+11C>G
|
|
ENST00000613243.1:c.1688+11C>G
|
ENSP00000478295.1:n.1688+11C>G
|
|
NM_001005242.2:c.1556+11C>G
|
NP_001005242.2:n.1556+11C>G
|
|
NM_004572.3:c.1688+11C>G , LRG_398t1:c.1688+11C>G
|
NP_004563.2:n.1688+11C>G
|
|
NM_001005242.3:c.1556+11C>G
MANE Select
|
NP_001005242.2:n.1556+11C>G
|
|
NM_004572.4:c.1688+11C>G
|
NP_004563.2:n.1688+11C>G
|
|