ENST00000328381.10:c.775A>T
MANE Select
|
ENSP00000328340.5:p.Ile259Phe
|
|
ENST00000324689.8:c.612A>T
|
ENSP00000323693.4:p.Pro204=
|
|
ENST00000328381.9:c.775A>T
|
ENSP00000328340.5:p.Ile259Phe
|
|
ENST00000443677.6:c.468A>T
|
ENSP00000411965.2:p.Pro156=
|
|
ENST00000535306.6:c.840A>T
|
ENSP00000440470.2:p.Pro280=
|
|
NM_001184992.1:c.840A>T
|
NP_001171921.1:p.Pro280=
|
|
NM_032322.3:c.775A>T
|
NP_115698.3:p.Ile259Phe
|
|
NM_197939.1:c.612A>T
|
NP_922921.1:p.Pro204=
|
|
XM_005258043.3:c.232A>T
|
XP_005258100.1:p.Ile78Phe
|
|
XM_006722138.2:c.454A>T
|
XP_006722201.1:p.Ile152Phe
|
|
XM_017025223.1:c.232A>T
|
XP_016880712.1:p.Ile78Phe
|
|
XM_024451000.1:c.232A>T
|
XP_024306768.1:p.Ile78Phe
|
|
XM_024451001.1:c.232A>T
|
XP_024306769.1:p.Ile78Phe
|
|
XR_002958076.1:n.1108A>T
|
|
|
XR_002958077.1:n.1043A>T
|
|
|
XR_002958078.1:n.880A>T
|
|
|
NM_032322.4:c.775A>T
MANE Select
|
NP_115698.3:p.Ile259Phe
|
|
NM_001184992.2:c.840A>T
|
NP_001171921.1:p.Pro280=
|
|
NM_197939.2:c.612A>T
|
NP_922921.1:p.Pro204=
|
|