ENST00000352909.8:c.204G>T
MANE Select
|
ENSP00000325951.4:p.Leu68=
|
|
ENST00000324155.8:c.91-63G>T
|
ENSP00000325831.3:n.91-63G>T
|
|
ENST00000333684.9:c.204G>T
|
ENSP00000328814.6:p.Leu68=
|
|
ENST00000352909.7:c.204G>T
|
ENSP00000325951.3:p.Leu68=
|
|
ENST00000381168.7:c.103-63G>T
|
ENSP00000370560.3:n.103-63G>T
|
|
ENST00000381175.5:c.285G>T
|
ENSP00000370567.1:p.Leu95=
|
|
ENST00000381178.5:c.297G>T
|
ENSP00000370571.1:p.Leu99=
|
|
NM_000360.3:c.204G>T
|
NP_000351.2:p.Leu68=
|
|
NM_199292.2:c.297G>T
|
NP_954986.2:p.Leu99=
|
|
NM_199293.2:c.285G>T
|
NP_954987.2:p.Leu95=
|
|
XM_011520335.1:c.216G>T
|
XP_011518637.1:p.Leu72=
|
|
XM_011520335.2:c.216G>T
|
XP_011518637.1:p.Leu72=
|
|
NM_000360.4:c.204G>T
MANE Select
|
NP_000351.2:p.Leu68=
|
|
NM_199292.3:c.297G>T
|
NP_954986.2:p.Leu99=
|
|
NM_199293.3:c.285G>T
|
NP_954987.2:p.Leu95=
|
|