ENST00000340855.11:c.1376A>T
MANE Select
|
ENSP00000339801.6:p.Glu459Val
|
|
ENST00000651111.1:c.743A>T
|
ENSP00000498395.1:p.Glu248Val
|
|
ENST00000340855.10:c.1376A>T
|
ENSP00000339801.6:p.Glu459Val
|
|
ENST00000422081.6:c.743A>T
|
ENSP00000477056.1:p.Glu248Val
|
|
NM_000202.6:c.1376A>T
|
NP_000193.1:p.Glu459Val
|
|
NM_001166550.2:c.1106A>T
|
NP_001160022.1:p.Glu369Val
|
|
NM_000202.7:c.1376A>T
|
NP_000193.1:p.Glu459Val
|
|
NM_001166550.3:c.1106A>T
|
NP_001160022.1:p.Glu369Val
|
|
NM_000202.8:c.1376A>T
MANE Select
|
NP_000193.1:p.Glu459Val
|
|
NM_001166550.4:c.1106A>T
|
NP_001160022.1:p.Glu369Val
|
|