ENST00000502773.6:c.*544T>A
MANE Select
|
ENSP00000422464.1:n.*544T>A
|
|
ENST00000274071.6:c.*1490T>A
|
ENSP00000274071.2:n.*1490T>A
|
|
ENST00000502773.5:c.*544T>A
|
ENSP00000422464.1:n.*544T>A
|
|
NM_016205.2:c.*544T>A
|
NP_057289.1:n.*544T>A
|
|
NR_036641.1:n.2134T>A
|
|
|
XM_011532124.1:c.*544T>A
|
XP_011530426.1:n.*544T>A
|
|
XM_011532125.1:c.*544T>A
|
XP_011530427.1:n.*544T>A
|
|
XM_011532124.2:c.*544T>A
|
XP_011530426.1:n.*544T>A
|
|
XM_017008455.1:c.*544T>A
|
XP_016863944.1:n.*544T>A
|
|
XM_017008456.2:c.*544T>A
|
XP_016863945.1:n.*544T>A
|
|
NM_016205.3:c.*544T>A
MANE Select
|
NP_057289.1:n.*544T>A
|
|
NR_036641.2:n.2539T>A
|
|
|