ENST00000352909.8:c.1253C>A
MANE Select
|
ENSP00000325951.4:p.Ala418Asp
|
|
ENST00000324155.8:c.*942C>A
|
ENSP00000325831.3:n.*942C>A
|
|
ENST00000333684.9:c.971C>A
|
ENSP00000328814.6:p.Ala324Asp
|
|
ENST00000352909.7:c.1253C>A
|
ENSP00000325951.3:p.Ala418Asp
|
|
ENST00000381175.5:c.1334C>A
|
ENSP00000370567.1:p.Ala445Asp
|
|
ENST00000381178.5:c.1346C>A
|
ENSP00000370571.1:p.Ala449Asp
|
|
NM_000360.3:c.1253C>A
|
NP_000351.2:p.Ala418Asp
|
|
NM_199292.2:c.1346C>A
|
NP_954986.2:p.Ala449Asp
|
|
NM_199293.2:c.1334C>A
|
NP_954987.2:p.Ala445Asp
|
|
XM_011520335.1:c.1265C>A
|
XP_011518637.1:p.Ala422Asp
|
|
XM_011520335.2:c.1265C>A
|
XP_011518637.1:p.Ala422Asp
|
|
NM_000360.4:c.1253C>A
MANE Select
|
NP_000351.2:p.Ala418Asp
|
|
NM_199292.3:c.1346C>A
|
NP_954986.2:p.Ala449Asp
|
|
NM_199293.3:c.1334C>A
|
NP_954987.2:p.Ala445Asp
|
|