ENST00000696962.1:c.138+874G>C
|
ENSP00000513001.1:n.138+874G>C
|
|
ENST00000422843.8:c.138+874G>C
MANE Select
|
ENSP00000398655.4:n.138+874G>C
|
|
ENST00000422843.7:c.138+874G>C
|
ENSP00000398655.3:n.138+874G>C
|
|
ENST00000517779.1:c.138+874G>C
|
ENSP00000431054.1:n.138+874G>C
|
|
ENST00000519402.5:n.273+874G>C
|
|
|
ENST00000520555.5:n.276+874G>C
|
|
|
ENST00000521769.5:c.-238+15843G>C
|
ENSP00000430327.1:n.-238+15843G>C
|
|
ENST00000522616.1:n.279+874G>C
|
|
|
NM_005546.3:c.138+874G>C , LRG_189t1:c.138+874G>C
|
NP_005537.3:n.138+874G>C
|
|
NM_005546.4:c.138+874G>C
MANE Select
|
NP_005537.3:n.138+874G>C
|
|