ENST00000344419.8:c.*496A=
MANE Select
|
ENSP00000343763.4:n.*496A=
|
|
ENST00000229447.9:c.*596A=
|
ENSP00000229447.5:n.*596A=
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|
ENST00000344419.7:c.*496A=
|
ENSP00000343763.3:n.*496A=
|
|
NM_001164694.1:c.*596A=
|
NP_001158166.1:n.*596A=
|
|
NM_001164695.1:c.*683A=
|
NP_001158167.1:n.*683A=
|
|
NM_203395.2:c.*496A=
|
NP_981932.1:n.*496A=
|
|
NM_001318495.1:c.*496A=
|
NP_001305424.1:n.*496A=
|
|
NR_134655.1:n.1679A=
|
|
|
NM_001164694.2:c.*596A=
|
NP_001158166.1:n.*596A=
|
|
NM_001164695.2:c.*683A=
|
NP_001158167.1:n.*683A=
|
|
NM_001318495.2:c.*496A=
|
NP_001305424.1:n.*496A=
|
|
NM_203395.3:c.*496A=
MANE Select
|
NP_981932.1:n.*496A=
|
|
NR_134655.2:n.1559A=
|
|
|