|
NM_015072.5:c.1487+1G>A
MANE Select
|
NP_055887.3:n.1487+1G>A
|
|
ENST00000298832.14:c.1487+1G>A
MANE Select
|
ENSP00000298832.9:n.1487+1G>A
|
|
NM_015072.4:c.1487+1G>A
|
NP_055887.3:n.1487+1G>A
|
|
ENST00000298832.13:c.1487+1G>A
|
ENSP00000298832.9:n.1487+1G>A
|
|
ENST00000554148.5:n.643+1G>A
|
|
|
ENST00000554510.5:c.-26+1G>A
|
ENSP00000451946.1:n.-26+1G>A
|
|
ENST00000555422.5:n.793+1G>A
|
|
|
ENST00000556893.5:c.101+1G>A
|
ENSP00000452524.1:n.101+1G>A
|
|
ENST00000556976.1:n.182+1G>A
|
|
|
ENST00000557636.5:c.1529+1G>A
|
ENSP00000450713.1:n.1529+1G>A
|