ENST00000650242.1:c.991C>T
MANE Select
|
ENSP00000497236.1:p.His331Tyr
|
|
ENST00000330807.9:c.991C>T
|
ENSP00000332369.5:p.His331Tyr
|
|
ENST00000335854.8:c.880C>T
|
ENSP00000337131.4:p.His294Tyr
|
|
ENST00000396198.7:c.952C>T
|
ENSP00000379501.3:p.His318Tyr
|
|
ENST00000498636.1:n.282C>T
|
|
|
NM_000032.4:c.991C>T
|
NP_000023.2:p.His331Tyr
|
|
NM_001037967.3:c.880C>T
|
NP_001033056.1:p.His294Tyr
|
|
NM_001037968.3:c.952C>T
|
NP_001033057.1:p.His318Tyr
|
|
XM_005261995.2:c.1063C>T
|
XP_005262052.1:p.His355Tyr
|
|
XM_011530771.1:c.130C>T
|
XP_011529073.1:p.His44Tyr
|
|
NM_000032.5:c.991C>T
MANE Select
|
NP_000023.2:p.His331Tyr
|
|
NM_001037967.4:c.880C>T
|
NP_001033056.1:p.His294Tyr
|
|
NM_001037968.4:c.952C>T
|
NP_001033057.1:p.His318Tyr
|
|