ENST00000258385.8:c.1222C>T
MANE Select
|
ENSP00000258385.3:p.His408Tyr
|
|
ENST00000258385.7:c.1222C>T
|
ENSP00000258385.3:p.His408Tyr
|
|
ENST00000441621.6:c.*404C>T
|
ENSP00000408819.2:n.*404C>T
|
|
ENST00000446616.1:c.*863C>T
|
ENSP00000410801.1:n.*863C>T
|
|
ENST00000543200.5:c.1177C>T
|
ENSP00000438380.1:p.His393Tyr
|
|
NM_000751.2:c.1222C>T
|
NP_000742.1:p.His408Tyr
|
|
NM_001256657.1:c.1177C>T
|
NP_001243586.1:p.His393Tyr
|
|
NM_001311195.1:c.640C>T
|
NP_001298124.1:p.His214Tyr
|
|
NM_001311196.1:c.919C>T
|
NP_001298125.1:p.His307Tyr
|
|
NR_046333.1:c.-4294966329C>T
|
|
|
NR_046334.1:c.-4294966050C>T
|
|
|
XM_011510524.1:c.841C>T
|
XP_011508826.1:p.His281Tyr
|
|
XM_011510524.2:c.841C>T
|
XP_011508826.1:p.His281Tyr
|
|
NM_000751.3:c.1222C>T
MANE Select
|
NP_000742.1:p.His408Tyr
|
|
NM_001311195.2:c.640C>T
|
NP_001298124.1:p.His214Tyr
|
|
NM_001311196.2:c.919C>T
|
NP_001298125.1:p.His307Tyr
|
|
NM_001256657.2:c.1177C>T
|
NP_001243586.1:p.His393Tyr
|
|