ENST00000409134.8:c.*1672A>G
MANE Select
|
ENSP00000387123.3:n.*1672A>G
|
|
ENST00000635851.1:c.1564-2305A>G
|
|
|
ENST00000637782.1:c.1565+3031A>G
|
ENSP00000490024.1:n.1565+3031A>G
|
|
ENST00000409134.7:c.*1672A>G
|
ENSP00000387123.3:n.*1672A>G
|
|
ENST00000447989.6:c.*1672A>G
|
ENSP00000414132.2:n.*1672A>G
|
|
NM_001182.4:c.*1672A>G
|
NP_001173.2:n.*1672A>G
|
|
NM_001201377.1:c.*1672A>G
|
NP_001188306.1:n.*1672A>G
|
|
NM_001202404.1:c.*1672A>G
|
NP_001189333.1:n.*1672A>G
|
|
NM_001182.5:c.*1672A>G
MANE Select
|
NP_001173.2:n.*1672A>G
|
|
NM_001201377.2:c.*1672A>G
|
NP_001188306.1:n.*1672A>G
|
|
NM_001202404.2:c.*1672A>G
|
NP_001189333.2:n.*1672A>G
|
|