ENST00000352909.8:c.706T>C
MANE Select
|
ENSP00000325951.4:p.Tyr236His
|
|
ENST00000324155.8:c.*395T>C
|
ENSP00000325831.3:n.*395T>C
|
|
ENST00000333684.9:c.695+413T>C
|
ENSP00000328814.6:n.695+413T>C
|
|
ENST00000352909.7:c.706T>C
|
ENSP00000325951.3:p.Tyr236His
|
|
ENST00000381168.7:c.*426T>C
|
ENSP00000370560.3:n.*426T>C
|
|
ENST00000381175.5:c.787T>C
|
ENSP00000370567.1:p.Tyr263His
|
|
ENST00000381178.5:c.799T>C
|
ENSP00000370571.1:p.Tyr267His
|
|
ENST00000412076.1:c.135+413T>C
|
|
|
ENST00000416223.5:c.136-254T>C
|
|
|
ENST00000469226.1:n.835T>C
|
|
|
ENST00000479437.5:n.255T>C
|
|
|
NM_000360.3:c.706T>C
|
NP_000351.2:p.Tyr236His
|
|
NM_199292.2:c.799T>C
|
NP_954986.2:p.Tyr267His
|
|
NM_199293.2:c.787T>C
|
NP_954987.2:p.Tyr263His
|
|
XM_011520335.1:c.718T>C
|
XP_011518637.1:p.Tyr240His
|
|
XM_011520335.2:c.718T>C
|
XP_011518637.1:p.Tyr240His
|
|
NM_000360.4:c.706T>C
MANE Select
|
NP_000351.2:p.Tyr236His
|
|
NM_199292.3:c.799T>C
|
NP_954986.2:p.Tyr267His
|
|
NM_199293.3:c.787T>C
|
NP_954987.2:p.Tyr263His
|
|