ENST00000320650.9:c.*316A>G
MANE Select
|
ENSP00000323505.4:n.*316A>G
|
|
ENST00000296545.11:c.*316A>G
|
ENSP00000296545.7:n.*316A>G
|
|
ENST00000320650.8:c.*316A>G
|
ENSP00000323505.4:n.*316A>G
|
|
ENST00000394159.2:c.724A>G
|
ENSP00000377714.1:n.724A>G
|
|
ENST00000477265.5:c.*316A>G
|
ENSP00000436914.1:n.*316A>G
|
|
ENST00000514653.5:c.*316A>G
|
ENSP00000422271.1:n.*316A>G
|
|
NM_000585.4:c.*316A>G
|
NP_000576.1:n.*316A>G
|
|
NM_172175.2:c.*316A>G
|
NP_751915.1:n.*316A>G
|
|
NR_037840.2:n.1655A>G
|
|
|
NM_000585.5:c.*316A>G
MANE Select
|
NP_000576.1:n.*316A>G
|
|
NM_172175.3:c.*316A>G
|
NP_751915.1:n.*316A>G
|
|
NR_037840.3:n.1668A>G
|
|
|