ENST00000352909.8:c.849G>T
MANE Select
|
ENSP00000325951.4:p.Thr283=
|
|
ENST00000324155.8:c.*538G>T
|
ENSP00000325831.3:n.*538G>T
|
|
ENST00000333684.9:c.696-212G>T
|
ENSP00000328814.6:n.696-212G>T
|
|
ENST00000352909.7:c.849G>T
|
ENSP00000325951.3:p.Thr283=
|
|
ENST00000381168.7:c.*569G>T
|
ENSP00000370560.3:n.*569G>T
|
|
ENST00000381175.5:c.930G>T
|
ENSP00000370567.1:p.Thr310=
|
|
ENST00000381178.5:c.942G>T
|
ENSP00000370571.1:p.Thr314=
|
|
ENST00000412076.1:c.136-212G>T
|
|
|
ENST00000416223.5:c.143G>T
|
|
|
ENST00000461172.1:n.14G>T
|
|
|
ENST00000479437.5:n.398G>T
|
|
|
NM_000360.3:c.849G>T
|
NP_000351.2:p.Thr283=
|
|
NM_199292.2:c.942G>T
|
NP_954986.2:p.Thr314=
|
|
NM_199293.2:c.930G>T
|
NP_954987.2:p.Thr310=
|
|
XM_011520335.1:c.861G>T
|
XP_011518637.1:p.Thr287=
|
|
XM_011520335.2:c.861G>T
|
XP_011518637.1:p.Thr287=
|
|
NM_000360.4:c.849G>T
MANE Select
|
NP_000351.2:p.Thr283=
|
|
NM_199292.3:c.942G>T
|
NP_954986.2:p.Thr314=
|
|
NM_199293.3:c.930G>T
|
NP_954987.2:p.Thr310=
|
|