ENST00000261951.9:c.*4049C>A
MANE Select
|
ENSP00000261951.4:n.*4049C>A
|
|
ENST00000393356.7:c.*4049C>A
|
ENSP00000377024.1:n.*4049C>A
|
|
ENST00000261951.8:c.*4049C>A
|
ENSP00000261951.4:n.*4049C>A
|
|
ENST00000393356.5:c.*4049C>A
|
ENSP00000377024.1:n.*4049C>A
|
|
ENST00000618123.4:c.*4049C>A
|
ENSP00000481893.1:n.*4049C>A
|
|
NM_001303241.1:c.*4049C>A
|
NP_001290170.1:n.*4049C>A
|
|
XM_005265953.1:c.*4049C>A
|
XP_005266010.1:n.*4049C>A
|
|
XM_011534605.1:c.*4049C>A
|
XP_011532907.1:n.*4049C>A
|
|
XM_011534606.1:c.*4049C>A
|
XP_011532908.1:n.*4049C>A
|
|
XM_011534607.1:c.*4049C>A
|
XP_011532909.1:n.*4049C>A
|
|
XM_011534608.1:c.*4233C>A
|
XP_011532910.1:n.*4233C>A
|
|
XM_017009672.1:c.*4233C>A
|
XP_016865161.1:n.*4233C>A
|
|
XR_001742163.1:n.5934C>A
|
|
|
XR_001742164.1:n.5919C>A
|
|
|
NM_001303241.2:c.*4049C>A
|
NP_001290170.1:n.*4049C>A
|
|
NM_001370472.1:c.*4049C>A
MANE Select
|
NP_001357401.1:n.*4049C>A
|
|
NM_001370473.1:c.*4049C>A
|
NP_001357402.1:n.*4049C>A
|
|
NM_001370474.1:c.*4049C>A
|
NP_001357403.1:n.*4049C>A
|
|
NR_163437.1:n.6214C>A
|
|
|
NR_163438.1:n.5955C>A
|
|
|