ENST00000401061.9:c.665_668delinsACTT
MANE Select
|
ENSP00000383840.4:p.Tyr222=
|
|
ENST00000401061.8:c.665_668delinsACTT
|
ENSP00000383840.4:p.Tyr222=
|
|
ENST00000616135.1:c.494_497delinsACTT
|
ENSP00000478859.1:p.Tyr165=
|
|
NM_015506.2:c.665_668delinsACTT
|
NP_056321.2:p.Tyr222=
|
|
XM_005270724.3:c.470_473delinsACTT
|
XP_005270781.1:p.Tyr157=
|
|
XM_011541204.1:c.494_497delinsACTT
|
XP_011539506.1:p.Tyr165=
|
|
NM_001330540.1:c.494_497delinsACTT
|
NP_001317469.1:p.Tyr165=
|
|
XM_005270724.5:c.470_473delinsACTT
|
XP_005270781.1:p.Tyr157=
|
|
NM_015506.3:c.665_668delinsACTT
MANE Select
|
NP_056321.2:p.Tyr222=
|
|
NM_001330540.2:c.494_497delinsACTT
|
NP_001317469.1:p.Tyr165=
|
|