ENST00000426263.10:c.728A>T
MANE Select
|
ENSP00000416293.2:p.Glu243Val
|
|
ENST00000669445.1:c.58A>T
|
|
|
ENST00000674765.1:c.728A>T
|
ENSP00000501811.1:p.Glu243Val
|
|
ENST00000675112.1:n.751A>T
|
|
|
ENST00000676254.1:n.1177A>T
|
|
|
ENST00000426263.7:c.728A>T
|
ENSP00000416293.2:p.Glu243Val
|
|
ENST00000439722.2:c.607A>T
|
ENSP00000395521.2:n.607A>T
|
|
ENST00000475162.3:c.415+894A>T
|
|
|
ENST00000630287.2:c.*43A>T
|
ENSP00000486694.1:n.*43A>T
|
|
NM_006516.2:c.728A>T
|
NP_006507.2:p.Glu243Val
|
|
NM_006516.3:c.728A>T
|
NP_006507.2:p.Glu243Val
|
|
NM_006516.4:c.728A>T
MANE Select
|
NP_006507.2:p.Glu243Val
|
|