ENST00000352909.8:c.1015C>T
MANE Select
|
ENSP00000325951.4:p.Leu339=
|
|
ENST00000324155.8:c.*704C>T
|
ENSP00000325831.3:n.*704C>T
|
|
ENST00000333684.9:c.733C>T
|
ENSP00000328814.6:p.Leu245=
|
|
ENST00000352909.7:c.1015C>T
|
ENSP00000325951.3:p.Leu339=
|
|
ENST00000381168.7:c.*735C>T
|
ENSP00000370560.3:n.*735C>T
|
|
ENST00000381175.5:c.1096C>T
|
ENSP00000370567.1:p.Leu366=
|
|
ENST00000381178.5:c.1108C>T
|
ENSP00000370571.1:p.Leu370=
|
|
ENST00000412076.1:c.173C>T
|
|
|
ENST00000416223.5:c.309C>T
|
|
|
ENST00000461172.1:n.180C>T
|
|
|
ENST00000479437.5:n.564C>T
|
|
|
NM_000360.3:c.1015C>T
|
NP_000351.2:p.Leu339=
|
|
NM_199292.2:c.1108C>T
|
NP_954986.2:p.Leu370=
|
|
NM_199293.2:c.1096C>T
|
NP_954987.2:p.Leu366=
|
|
XM_011520335.1:c.1027C>T
|
XP_011518637.1:p.Leu343=
|
|
XM_011520335.2:c.1027C>T
|
XP_011518637.1:p.Leu343=
|
|
NM_000360.4:c.1015C>T
MANE Select
|
NP_000351.2:p.Leu339=
|
|
NM_199292.3:c.1108C>T
|
NP_954986.2:p.Leu370=
|
|
NM_199293.3:c.1096C>T
|
NP_954987.2:p.Leu366=
|
|