ENST00000572705.2:c.*343A>T
MANE Select
|
ENSP00000459962.1:n.*343A>T
|
|
ENST00000650505.1:c.*1344A>T
|
ENSP00000497337.1:n.*1344A>T
|
|
ENST00000399756.8:c.*343A>T
|
ENSP00000382659.4:n.*343A>T
|
|
ENST00000399759.7:c.*343A>T
|
ENSP00000382661.3:n.*343A>T
|
|
ENST00000571088.5:c.*343A>T
|
ENSP00000461007.1:n.*343A>T
|
|
ENST00000572705.1:c.*343A>T
|
ENSP00000459962.1:n.*343A>T
|
|
NM_018727.5:c.*343A>T
|
NP_061197.4:n.*343A>T
|
|
NM_080704.3:c.*343A>T
|
NP_542435.2:n.*343A>T
|
|
NM_080705.3:c.*343A>T
|
NP_542436.2:n.*343A>T
|
|
NM_080706.3:c.*343A>T
|
NP_542437.2:n.*343A>T
|
|
NM_080704.4:c.*343A>T
MANE Select
|
NP_542435.2:n.*343A>T
|
|
NM_080705.4:c.*343A>T
|
NP_542436.2:n.*343A>T
|
|