ENST00000351513.7:c.*351A>G
MANE Select
|
ENSP00000276651.2:n.*351A>G
|
|
ENST00000351513.6:c.*351A>G
|
ENSP00000276651.2:n.*351A>G
|
|
ENST00000520806.1:n.565A>G
|
|
|
ENST00000521601.1:n.328+1677A>G
|
|
|
ENST00000533874.1:c.410A>G
|
|
|
NM_001385.2:c.*351A>G
|
NP_001376.1:n.*351A>G
|
|
XM_005250818.2:c.*351A>G
|
XP_005250875.1:n.*351A>G
|
|
XM_006716518.2:c.*351A>G
|
XP_006716581.1:n.*351A>G
|
|
XM_005250818.3:c.*351A>G
|
XP_005250875.1:n.*351A>G
|
|
XM_006716518.3:c.*351A>G
|
XP_006716581.1:n.*351A>G
|
|
XM_024447087.1:c.*888A>G
|
XP_024302855.1:n.*888A>G
|
|
XR_001745489.1:n.2510A>G
|
|
|
XR_001745490.2:n.2402A>G
|
|
|
NM_001385.3:c.*351A>G
MANE Select
|
NP_001376.1:n.*351A>G
|
|