ENST00000343139.11:c.331+184C>G
MANE Select
|
ENSP00000339398.5:n.331+184C>G
|
|
ENST00000343139.9:c.331+184C>G
|
ENSP00000339398.5:n.331+184C>G
|
|
ENST00000374949.2:c.331+184C>G
|
ENSP00000364087.2:n.331+184C>G
|
|
ENST00000395363.5:c.331+184C>G
|
ENSP00000378767.1:n.331+184C>G
|
|
ENST00000460633.1:n.359+184C>G
|
|
|
ENST00000482745.5:c.*1163+184C>G
|
ENSP00000436546.1:n.*1163+184C>G
|
|
ENST00000496318.5:c.331+184C>G
|
ENSP00000437302.1:n.331+184C>G
|
|
NM_002122.3:c.331+184C>G
|
NP_002113.2:n.331+184C>G
|
|
XM_006715079.2:c.331+184C>G
|
XP_006715142.1:n.331+184C>G
|
|
XM_006715079.4:c.331+184C>G
|
XP_006715142.1:n.331+184C>G
|
|
XR_001744085.1:n.86+846G>C
|
|
|
NM_002122.5:c.331+184C>G
MANE Select
|
NP_002113.2:n.331+184C>G
|
|