ENST00000352909.8:c.826T=
MANE Select
|
ENSP00000325951.4:p.Ser276=
|
|
ENST00000324155.8:c.*515T=
|
ENSP00000325831.3:n.*515T=
|
|
ENST00000333684.9:c.696-353T=
|
ENSP00000328814.6:n.696-353T=
|
|
ENST00000352909.7:c.826T=
|
ENSP00000325951.3:p.Ser276=
|
|
ENST00000381168.7:c.*546T=
|
ENSP00000370560.3:n.*546T=
|
|
ENST00000381175.5:c.907T=
|
ENSP00000370567.1:p.Ser303=
|
|
ENST00000381178.5:c.919T=
|
ENSP00000370571.1:p.Ser307=
|
|
ENST00000412076.1:c.136-353T=
|
|
|
ENST00000416223.5:c.136-134T=
|
|
|
ENST00000469226.1:n.955T=
|
|
|
ENST00000479437.5:n.375T=
|
|
|
NM_000360.3:c.826T=
|
NP_000351.2:p.Ser276=
|
|
NM_199292.2:c.919T=
|
NP_954986.2:p.Ser307=
|
|
NM_199293.2:c.907T=
|
NP_954987.2:p.Ser303=
|
|
XM_011520335.1:c.838T=
|
XP_011518637.1:p.Ser280=
|
|
XM_011520335.2:c.838T=
|
XP_011518637.1:p.Ser280=
|
|
NM_000360.4:c.826T=
MANE Select
|
NP_000351.2:p.Ser276=
|
|
NM_199292.3:c.919T=
|
NP_954986.2:p.Ser307=
|
|
NM_199293.3:c.907T=
|
NP_954987.2:p.Ser303=
|
|