ENST00000352909.8:c.780C>T
MANE Select
|
ENSP00000325951.4:p.Arg260=
|
|
ENST00000324155.8:c.*469C>T
|
ENSP00000325831.3:n.*469C>T
|
|
ENST00000333684.9:c.696-399C>T
|
ENSP00000328814.6:n.696-399C>T
|
|
ENST00000352909.7:c.780C>T
|
ENSP00000325951.3:p.Arg260=
|
|
ENST00000381168.7:c.*500C>T
|
ENSP00000370560.3:n.*500C>T
|
|
ENST00000381175.5:c.861C>T
|
ENSP00000370567.1:p.Arg287=
|
|
ENST00000381178.5:c.873C>T
|
ENSP00000370571.1:p.Arg291=
|
|
ENST00000412076.1:c.136-399C>T
|
|
|
ENST00000416223.5:c.136-180C>T
|
|
|
ENST00000469226.1:n.909C>T
|
|
|
ENST00000479437.5:n.329C>T
|
|
|
NM_000360.3:c.780C>T
|
NP_000351.2:p.Arg260=
|
|
NM_199292.2:c.873C>T
|
NP_954986.2:p.Arg291=
|
|
NM_199293.2:c.861C>T
|
NP_954987.2:p.Arg287=
|
|
XM_011520335.1:c.792C>T
|
XP_011518637.1:p.Arg264=
|
|
XM_011520335.2:c.792C>T
|
XP_011518637.1:p.Arg264=
|
|
NM_000360.4:c.780C>T
MANE Select
|
NP_000351.2:p.Arg260=
|
|
NM_199292.3:c.873C>T
|
NP_954986.2:p.Arg291=
|
|
NM_199293.3:c.861C>T
|
NP_954987.2:p.Arg287=
|
|