ENST00000355417.7:c.48+8682A>G
(CCDC69)
MANE Select
|
ENSP00000347586.2:n.48+8682A>G
|
|
ENST00000355417.6:c.48+8682A>G
(CCDC69)
|
ENSP00000347586.2:n.48+8682A>G
|
|
ENST00000521308.5:n.171+8682A>G
(CCDC69)
|
|
|
ENST00000523466.5:c.126+2352T>C
(GM2A)
|
ENSP00000429100.1:n.126+2352T>C
|
|
NM_015621.2:c.48+8682A>G
(CCDC69)
|
NP_056436.2:n.48+8682A>G
|
|
XR_944412.1:n.623+2352T>C
|
|
|
XR_944414.1:n.623+2352T>C
|
|
|
XR_944415.1:n.623+2352T>C
|
|
|
XM_017010135.1:c.126+2352T>C
|
XP_016865624.1:n.126+2352T>C
|
|
XM_017010136.1:c.126+2352T>C
|
XP_016865625.1:n.126+2352T>C
|
|
XR_944414.2:n.638+2352T>C
|
|
|
XR_944415.2:n.638+2352T>C
|
|
|
NM_015621.3:c.48+8682A>G
(CCDC69)
MANE Select
|
NP_056436.2:n.48+8682A>G
|
|
NR_160730.1:n.257+2352T>C
|
|
|