ENST00000352909.8:c.713C>T
MANE Select
|
ENSP00000325951.4:p.Thr238Met
|
|
ENST00000324155.8:c.*402C>T
|
ENSP00000325831.3:n.*402C>T
|
|
ENST00000333684.9:c.695+420C>T
|
ENSP00000328814.6:n.695+420C>T
|
|
ENST00000352909.7:c.713C>T
|
ENSP00000325951.3:p.Thr238Met
|
|
ENST00000381168.7:c.*433C>T
|
ENSP00000370560.3:n.*433C>T
|
|
ENST00000381175.5:c.794C>T
|
ENSP00000370567.1:p.Thr265Met
|
|
ENST00000381178.5:c.806C>T
|
ENSP00000370571.1:p.Thr269Met
|
|
ENST00000412076.1:c.135+420C>T
|
|
|
ENST00000416223.5:c.136-247C>T
|
|
|
ENST00000469226.1:n.842C>T
|
|
|
ENST00000479437.5:n.262C>T
|
|
|
NM_000360.3:c.713C>T
|
NP_000351.2:p.Thr238Met
|
|
NM_199292.2:c.806C>T
|
NP_954986.2:p.Thr269Met
|
|
NM_199293.2:c.794C>T
|
NP_954987.2:p.Thr265Met
|
|
XM_011520335.1:c.725C>T
|
XP_011518637.1:p.Thr242Met
|
|
XM_011520335.2:c.725C>T
|
XP_011518637.1:p.Thr242Met
|
|
NM_000360.4:c.713C>T
MANE Select
|
NP_000351.2:p.Thr238Met
|
|
NM_199292.3:c.806C>T
|
NP_954986.2:p.Thr269Met
|
|
NM_199293.3:c.794C>T
|
NP_954987.2:p.Thr265Met
|
|