ENST00000374737.9:c.*388T>G
MANE Select
|
ENSP00000363869.4:n.*388T>G
|
|
ENST00000651578.1:c.*838T>G
|
ENSP00000498502.1:n.*838T>G
|
|
ENST00000374737.8:c.*388T>G
|
ENSP00000363869.4:n.*388T>G
|
|
ENST00000412866.2:c.*388T>G
|
ENSP00000394143.2:n.*388T>G
|
|
ENST00000427538.5:c.1033T>G
|
|
|
ENST00000455586.6:c.*962T>G
|
ENSP00000411581.2:n.*962T>G
|
|
NM_001100431.1:c.*388T>G
|
NP_001093901.1:n.*388T>G
|
|
NM_001184830.1:c.*962T>G
|
NP_001171759.1:n.*962T>G
|
|
NM_001184831.1:c.*962T>G
|
NP_001171760.1:n.*962T>G
|
|
NM_001257403.1:c.*210T>G
|
NP_001244332.1:n.*210T>G
|
|
NM_007268.2:c.*388T>G
|
NP_009199.1:n.*388T>G
|
|
XM_017029251.2:c.*210T>G
|
XP_016884740.1:n.*210T>G
|
|
NM_007268.3:c.*388T>G
MANE Select
|
NP_009199.1:n.*388T>G
|
|
NM_001100431.2:c.*388T>G
|
NP_001093901.1:n.*388T>G
|
|
NM_001184831.2:c.*962T>G
|
NP_001171760.1:n.*962T>G
|
|
NM_001257403.2:c.*210T>G
|
NP_001244332.1:n.*210T>G
|
|
NM_001184830.2:c.*962T>G
|
NP_001171759.1:n.*962T>G
|
|