ENST00000352909.8:c.804T>A
MANE Select
|
ENSP00000325951.4:p.Asn268Lys
|
|
ENST00000324155.8:c.*493T>A
|
ENSP00000325831.3:n.*493T>A
|
|
ENST00000333684.9:c.696-375T>A
|
ENSP00000328814.6:n.696-375T>A
|
|
ENST00000352909.7:c.804T>A
|
ENSP00000325951.3:p.Asn268Lys
|
|
ENST00000381168.7:c.*524T>A
|
ENSP00000370560.3:n.*524T>A
|
|
ENST00000381175.5:c.885T>A
|
ENSP00000370567.1:p.Asn295Lys
|
|
ENST00000381178.5:c.897T>A
|
ENSP00000370571.1:p.Asn299Lys
|
|
ENST00000412076.1:c.136-375T>A
|
|
|
ENST00000416223.5:c.136-156T>A
|
|
|
ENST00000469226.1:n.933T>A
|
|
|
ENST00000479437.5:n.353T>A
|
|
|
NM_000360.3:c.804T>A
|
NP_000351.2:p.Asn268Lys
|
|
NM_199292.2:c.897T>A
|
NP_954986.2:p.Asn299Lys
|
|
NM_199293.2:c.885T>A
|
NP_954987.2:p.Asn295Lys
|
|
XM_011520335.1:c.816T>A
|
XP_011518637.1:p.Asn272Lys
|
|
XM_011520335.2:c.816T>A
|
XP_011518637.1:p.Asn272Lys
|
|
NM_000360.4:c.804T>A
MANE Select
|
NP_000351.2:p.Asn268Lys
|
|
NM_199292.3:c.897T>A
|
NP_954986.2:p.Asn299Lys
|
|
NM_199293.3:c.885T>A
|
NP_954987.2:p.Asn295Lys
|
|