ENST00000261647.10:c.*157A>G
MANE Select
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ENSP00000261647.5:n.*157A>G
|
|
ENST00000261647.9:c.*157A>G
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ENSP00000261647.5:n.*157A>G
|
|
ENST00000465567.1:n.1694A>G
|
|
|
ENST00000470649.1:c.247+977A>G
|
ENSP00000465627.1:n.247+977A>G
|
|
ENST00000475723.5:c.1484A>G
|
|
|
ENST00000481107.1:n.1968A>G
|
|
|
NM_001271420.1:c.*157A>G
|
NP_001258349.1:n.*157A>G
|
|
NM_017775.3:c.*157A>G
|
NP_060245.3:n.*157A>G
|
|
XM_017024801.2:c.994+977A>G
|
XP_016880290.2:n.994+977A>G
|
|
XM_017024802.2:c.994+977A>G
|
XP_016880291.2:n.994+977A>G
|
|
NM_017775.4:c.*157A>G
MANE Select
|
NP_060245.3:n.*157A>G
|
|
NM_001271420.2:c.*157A>G
|
NP_001258349.1:n.*157A>G
|
|