ENST00000352909.8:c.760G>T
MANE Select
|
ENSP00000325951.4:p.Ala254Ser
|
|
ENST00000324155.8:c.*449G>T
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ENSP00000325831.3:n.*449G>T
|
|
ENST00000333684.9:c.696-419G>T
|
ENSP00000328814.6:n.696-419G>T
|
|
ENST00000352909.7:c.760G>T
|
ENSP00000325951.3:p.Ala254Ser
|
|
ENST00000381168.7:c.*480G>T
|
ENSP00000370560.3:n.*480G>T
|
|
ENST00000381175.5:c.841G>T
|
ENSP00000370567.1:p.Ala281Ser
|
|
ENST00000381178.5:c.853G>T
|
ENSP00000370571.1:p.Ala285Ser
|
|
ENST00000412076.1:c.136-419G>T
|
|
|
ENST00000416223.5:c.136-200G>T
|
|
|
ENST00000469226.1:n.889G>T
|
|
|
ENST00000479437.5:n.309G>T
|
|
|
NM_000360.3:c.760G>T
|
NP_000351.2:p.Ala254Ser
|
|
NM_199292.2:c.853G>T
|
NP_954986.2:p.Ala285Ser
|
|
NM_199293.2:c.841G>T
|
NP_954987.2:p.Ala281Ser
|
|
XM_011520335.1:c.772G>T
|
XP_011518637.1:p.Ala258Ser
|
|
XM_011520335.2:c.772G>T
|
XP_011518637.1:p.Ala258Ser
|
|
NM_000360.4:c.760G>T
MANE Select
|
NP_000351.2:p.Ala254Ser
|
|
NM_199292.3:c.853G>T
|
NP_954986.2:p.Ala285Ser
|
|
NM_199293.3:c.841G>T
|
NP_954987.2:p.Ala281Ser
|
|