ENST00000261647.10:c.*1292T>G
MANE Select
|
ENSP00000261647.5:n.*1292T>G
|
|
ENST00000261647.9:c.*1292T>G
|
ENSP00000261647.5:n.*1292T>G
|
|
ENST00000470649.1:c.247+2112T>G
|
ENSP00000465627.1:n.247+2112T>G
|
|
NM_001271420.1:c.*1292T>G
|
NP_001258349.1:n.*1292T>G
|
|
NM_017775.3:c.*1292T>G
|
NP_060245.3:n.*1292T>G
|
|
XM_017024801.2:c.994+2112T>G
|
XP_016880290.2:n.994+2112T>G
|
|
XM_017024802.2:c.994+2112T>G
|
XP_016880291.2:n.994+2112T>G
|
|
NM_017775.4:c.*1292T>G
MANE Select
|
NP_060245.3:n.*1292T>G
|
|
NM_001271420.2:c.*1292T>G
|
NP_001258349.1:n.*1292T>G
|
|