ENST00000710265.1:c.*2477G>T
|
ENSP00000518161.1:n.*2477G>T
|
|
ENST00000688158.2:n.4183G>T
|
|
|
ENST00000706954.1:c.*2236G>T
|
ENSP00000516674.1:n.*2236G>T
|
|
ENST00000706955.1:c.*3483G>T
|
ENSP00000516675.1:n.*3483G>T
|
|
ENST00000688158.1:c.*3559G>T
|
ENSP00000509254.1:n.*3559G>T
|
|
ENST00000693560.1:c.*2236G>T
|
ENSP00000509861.1:n.*2236G>T
|
|
ENST00000371953.8:c.*2236G>T
MANE Select
|
ENSP00000361021.3:n.*2236G>T
|
|
ENST00000371953.7:c.*2236G>T
|
ENSP00000361021.3:n.*2236G>T
|
|
NM_000314.5:c.*2236G>T
|
NP_000305.3:n.*2236G>T
|
|
NM_000314.6:c.*2236G>T
|
NP_000305.3:n.*2236G>T
|
|
NM_001304717.2:c.*2236G>T
|
NP_001291646.2:n.*2236G>T
|
|
NM_001304718.1:c.*2236G>T
|
NP_001291647.1:n.*2236G>T
|
|
XM_006717926.2:c.*2236G>T
|
XP_006717989.1:n.*2236G>T
|
|
XM_011539982.1:c.*2236G>T
|
XP_011538284.1:n.*2236G>T
|
|
XR_945791.1:n.4018G>T
|
|
|
NM_000314.7:c.*2236G>T
|
NP_000305.3:n.*2236G>T
|
|
NM_001304717.5:c.*2236G>T
|
NP_001291646.4:n.*2236G>T
|
|
NM_001304718.2:c.*2236G>T
|
NP_001291647.1:n.*2236G>T
|
|
NM_000314.8:c.*2236G>T
MANE Select
|
NP_000305.3:n.*2236G>T
|
|