|
NM_015512.5:c.1656+1G>C
MANE Select
|
NP_056327.4:n.1656+1G>C
|
|
ENST00000420323.7:c.1656+1G>C
MANE Select
|
ENSP00000401514.2:n.1656+1G>C
|
|
NM_015512.4:c.1656+1G>C
|
NP_056327.4:n.1656+1G>C
|
|
ENST00000420323.6:c.1656+1G>C
|
ENSP00000401514.2:n.1656+1G>C
|
|
ENST00000486752.5:n.1917+1G>C
|
|
|
ENST00000497875.1:n.1821+1G>C
|
|
|
XM_011533577.1:c.1656+1G>C
|
XP_011531879.1:n.1656+1G>C
|
|
XM_017006129.1:c.1656+1G>C
|
XP_016861618.1:n.1656+1G>C
|
|
XM_017006130.1:c.1656+1G>C
|
XP_016861619.1:n.1656+1G>C
|
|
XM_017006131.1:c.1656+1G>C
|
XP_016861620.1:n.1656+1G>C
|
|
XM_017006132.1:c.1656+1G>C
|
XP_016861621.1:n.1656+1G>C
|
|
XM_017006133.1:c.1656+1G>C
|
XP_016861622.1:n.1656+1G>C
|
|
XR_001740098.1:n.4805+1G>C
|
|
|
XR_001740099.1:n.4805+1G>C
|
|