ENST00000357103.5:c.*1925A>G
MANE Select
|
ENSP00000349616.4:n.*1925A>G
|
|
ENST00000357103.4:c.*1925A>G
|
ENSP00000349616.4:n.*1925A>G
|
|
NM_024551.2:c.*1925A>G
|
NP_078827.2:n.*1925A>G
|
|
XM_005253789.1:c.*1925A>G
|
XP_005253846.1:n.*1925A>G
|
|
XM_006719018.1:c.*1925A>G
|
XP_006719081.1:n.*1925A>G
|
|
XM_011521024.1:c.*1925A>G
|
XP_011519326.1:n.*1925A>G
|
|
XM_011521025.1:c.*1925A>G
|
XP_011519327.1:n.*1925A>G
|
|
XM_005253789.2:c.*1925A>G
|
XP_005253846.1:n.*1925A>G
|
|
XM_006719018.2:c.*1925A>G
|
XP_006719081.1:n.*1925A>G
|
|
XM_011521024.2:c.*1925A>G
|
XP_011519326.1:n.*1925A>G
|
|
NM_024551.3:c.*1925A>G
MANE Select
|
NP_078827.2:n.*1925A>G
|
|
NM_001375363.1:c.*1925A>G
|
NP_001362292.1:n.*1925A>G
|
|
NM_001375364.1:c.*1925A>G
|
NP_001362293.1:n.*1925A>G
|
|
NM_001375365.1:c.*1925A>G
|
NP_001362294.1:n.*1925A>G
|
|