ENST00000344419.8:c.*852G>T
MANE Select
|
ENSP00000343763.4:n.*852G>T
|
|
ENST00000229447.9:c.*952G>T
|
ENSP00000229447.5:n.*952G>T
|
|
ENST00000344419.7:c.*852G>T
|
ENSP00000343763.3:n.*852G>T
|
|
NM_001164694.1:c.*952G>T
|
NP_001158166.1:n.*952G>T
|
|
NM_001164695.1:c.*1039G>T
|
NP_001158167.1:n.*1039G>T
|
|
NM_203395.2:c.*852G>T
|
NP_981932.1:n.*852G>T
|
|
NM_001318495.1:c.*852G>T
|
NP_001305424.1:n.*852G>T
|
|
NR_134655.1:n.2035G>T
|
|
|
NM_001164694.2:c.*952G>T
|
NP_001158166.1:n.*952G>T
|
|
NM_001164695.2:c.*1039G>T
|
NP_001158167.1:n.*1039G>T
|
|
NM_001318495.2:c.*852G>T
|
NP_001305424.1:n.*852G>T
|
|
NM_203395.3:c.*852G>T
MANE Select
|
NP_981932.1:n.*852G>T
|
|
NR_134655.2:n.1915G>T
|
|
|