ENST00000399506.9:c.*2377A>G
MANE Select
|
ENSP00000382425.2:n.*2377A>G
|
|
NM_001128827.3:c.*2377A>G
|
NP_001122299.1:n.*2377A>G
|
|
NM_001321075.3:c.*2377A>G
MANE Select
|
NP_001308004.1:n.*2377A>G
|
|
NM_001321076.2:c.*2377A>G
|
NP_001308005.1:n.*2377A>G
|
|
NM_001321077.2:c.*2377A>G
|
NP_001308006.1:n.*2377A>G
|
|
NM_001369566.2:c.*2377A>G
|
NP_001356495.1:n.*2377A>G
|
|
NM_001128827.4:c.*2377A>G
|
NP_001122299.1:n.*2377A>G
|
|
NM_001321076.3:c.*2377A>G
|
NP_001308005.1:n.*2377A>G
|
|
NM_001321077.3:c.*2377A>G
|
NP_001308006.1:n.*2377A>G
|
|
NM_001369566.3:c.*2377A>G
|
NP_001356495.1:n.*2377A>G
|
|