ENST00000355480.10:c.1344G=
|
ENSP00000347665.5:p.Ala448=
|
|
ENST00000651438.1:c.804G=
MANE Select
|
ENSP00000498485.1:p.Ala268=
|
|
ENST00000355480.9:c.1344G=
|
ENSP00000347665.5:p.Ala448=
|
|
ENST00000359759.8:c.2049G=
|
ENSP00000352798.4:p.Ala683=
|
|
ENST00000400337.6:c.804G=
|
ENSP00000383191.2:p.Ala268=
|
|
NM_030582.3:c.1344G=
|
NP_085059.2:p.Ala448=
|
|
NM_130444.2:c.2049G=
|
NP_569711.2:p.Ala683=
|
|
NM_130445.3:c.804G=
|
NP_569712.2:p.Ala268=
|
|
NM_030582.4:c.1344G=
|
NP_085059.2:p.Ala448=
|
|
NM_130444.3:c.2049G=
|
NP_569711.2:p.Ala683=
|
|
NM_130445.4:c.804G=
|
NP_569712.2:p.Ala268=
|
|
NM_001379500.1:c.804G=
MANE Select
|
NP_001366429.1:p.Ala268=
|
|