ENST00000352909.8:c.707A>T
MANE Select
|
ENSP00000325951.4:p.Tyr236Phe
|
|
ENST00000324155.8:c.*396A>T
|
ENSP00000325831.3:n.*396A>T
|
|
ENST00000333684.9:c.695+414A>T
|
ENSP00000328814.6:n.695+414A>T
|
|
ENST00000352909.7:c.707A>T
|
ENSP00000325951.3:p.Tyr236Phe
|
|
ENST00000381168.7:c.*427A>T
|
ENSP00000370560.3:n.*427A>T
|
|
ENST00000381175.5:c.788A>T
|
ENSP00000370567.1:p.Tyr263Phe
|
|
ENST00000381178.5:c.800A>T
|
ENSP00000370571.1:p.Tyr267Phe
|
|
ENST00000412076.1:c.135+414A>T
|
|
|
ENST00000416223.5:c.136-253A>T
|
|
|
ENST00000469226.1:n.836A>T
|
|
|
ENST00000479437.5:n.256A>T
|
|
|
NM_000360.3:c.707A>T
|
NP_000351.2:p.Tyr236Phe
|
|
NM_199292.2:c.800A>T
|
NP_954986.2:p.Tyr267Phe
|
|
NM_199293.2:c.788A>T
|
NP_954987.2:p.Tyr263Phe
|
|
XM_011520335.1:c.719A>T
|
XP_011518637.1:p.Tyr240Phe
|
|
XM_011520335.2:c.719A>T
|
XP_011518637.1:p.Tyr240Phe
|
|
NM_000360.4:c.707A>T
MANE Select
|
NP_000351.2:p.Tyr236Phe
|
|
NM_199292.3:c.800A>T
|
NP_954986.2:p.Tyr267Phe
|
|
NM_199293.3:c.788A>T
|
NP_954987.2:p.Tyr263Phe
|
|