ENST00000703608.1:c.*781G>A
|
ENSP00000515392.1:n.*781G>A
|
|
ENST00000703609.1:c.*43G>A
|
ENSP00000515393.1:n.*43G>A
|
|
ENST00000310144.11:c.*43G>A
MANE Select
|
ENSP00000310572.6:n.*43G>A
|
|
ENST00000310144.10:c.*43G>A
|
ENSP00000310572.6:n.*43G>A
|
|
ENST00000375812.8:c.*43G>A
|
ENSP00000364970.4:n.*43G>A
|
|
ENST00000578570.5:n.1674G>A
|
|
|
ENST00000579147.5:n.2579G>A
|
|
|
ENST00000580864.5:c.*43G>A
|
ENSP00000462495.1:n.*43G>A
|
|
ENST00000584657.1:n.569G>A
|
|
|
NM_001199163.1:c.*43G>A
|
NP_001186092.1:n.*43G>A
|
|
NM_002805.5:c.*43G>A
|
NP_002796.4:n.*43G>A
|
|
XM_006721980.1:c.*43G>A
|
XP_006722043.1:n.*43G>A
|
|
XR_934508.1:n.1353G>A
|
|
|
XM_024450840.1:c.*43G>A
|
XP_024306608.1:n.*43G>A
|
|
XM_024450841.1:c.*43G>A
|
XP_024306609.1:n.*43G>A
|
|
XR_934508.2:n.1340G>A
|
|
|
NM_002805.6:c.*43G>A
MANE Select
|
NP_002796.4:n.*43G>A
|
|
NM_001199163.2:c.*43G>A
|
NP_001186092.1:n.*43G>A
|
|