ENST00000529694.6:c.*31C>G
MANE Select
|
ENSP00000433295.1:n.*31C>G
|
|
ENST00000338350.4:c.*31C>G
|
ENSP00000339960.4:n.*31C>G
|
|
ENST00000529694.5:c.*31C>G
|
ENSP00000433295.1:n.*31C>G
|
|
NM_000890.3:c.*31C>G , LRG_333t1:c.*31C>G
|
NP_000881.3:n.*31C>G
|
|
XM_011542809.1:c.*31C>G
|
XP_011541111.1:n.*31C>G
|
|
XM_011542810.1:c.*31C>G
|
XP_011541112.1:n.*31C>G
|
|
NM_000890.4:c.*31C>G
|
NP_000881.3:n.*31C>G
|
|
NM_001354169.1:c.*31C>G
|
NP_001341098.1:n.*31C>G
|
|
XM_011542809.2:c.*31C>G
|
XP_011541111.1:n.*31C>G
|
|
XM_011542810.3:c.*31C>G
|
XP_011541112.1:n.*31C>G
|
|
NM_000890.5:c.*31C>G
MANE Select
|
NP_000881.3:n.*31C>G
|
|
NM_001354169.2:c.*31C>G
|
NP_001341098.1:n.*31C>G
|
|