ENST00000296522.11:c.522T>C
MANE Select
|
ENSP00000296522.6:p.Ser174=
|
|
ENST00000296521.11:c.499-1197T>C
|
ENSP00000296521.7:n.499-1197T>C
|
|
ENST00000296522.10:c.522T>C
|
ENSP00000296522.6:p.Ser174=
|
|
ENST00000422112.6:c.318T>C
|
ENSP00000398720.2:p.Ser106=
|
|
ENST00000506910.5:c.159T>C
|
ENSP00000423066.1:p.Ser53=
|
|
ENST00000508330.5:c.*151T>C
|
ENSP00000425741.1:n.*151T>C
|
|
ENST00000509512.1:n.171T>C
|
|
|
ENST00000510835.5:c.*284T>C
|
ENSP00000427699.1:n.*284T>C
|
|
ENST00000510901.5:c.159T>C
|
ENSP00000422418.1:p.Ser53=
|
|
ENST00000511499.5:n.306T>C
|
|
|
ENST00000514584.5:c.159T>C
|
ENSP00000423110.1:p.Ser53=
|
|
ENST00000541923.5:c.159T>C
|
ENSP00000438017.1:p.Ser53=
|
|
ENST00000542498.5:c.422-1197T>C
|
ENSP00000443644.1:n.422-1197T>C
|
|
NM_000860.5:c.522T>C
|
NP_000851.2:p.Ser174=
|
|
NM_001145816.2:c.499-1197T>C
|
NP_001139288.1:n.499-1197T>C
|
|
NM_001256301.1:c.159T>C
|
NP_001243230.1:p.Ser53=
|
|
NM_001256305.1:c.422-1197T>C
|
NP_001243234.1:n.422-1197T>C
|
|
NM_001256306.1:c.318T>C
|
NP_001243235.1:p.Ser106=
|
|
NM_001256307.1:c.159T>C
|
NP_001243236.1:p.Ser53=
|
|
NM_000860.6:c.522T>C
MANE Select
|
NP_000851.2:p.Ser174=
|
|
NM_001145816.3:c.499-1197T>C
|
NP_001139288.1:n.499-1197T>C
|
|
NM_001256305.2:c.422-1197T>C
|
NP_001243234.1:n.422-1197T>C
|
|
NM_001256306.2:c.318T>C
|
NP_001243235.1:p.Ser106=
|
|
NM_001256307.2:c.159T>C
|
NP_001243236.1:p.Ser53=
|
|