ENST00000426263.10:c.707A>T
MANE Select
|
ENSP00000416293.2:p.Asp236Val
|
|
ENST00000669445.1:c.57-20A>T
|
|
|
ENST00000674765.1:c.707A>T
|
ENSP00000501811.1:p.Asp236Val
|
|
ENST00000675112.1:n.730A>T
|
|
|
ENST00000676254.1:n.1156A>T
|
|
|
ENST00000426263.7:c.707A>T
|
ENSP00000416293.2:p.Asp236Val
|
|
ENST00000439722.2:c.586A>T
|
ENSP00000395521.2:n.586A>T
|
|
ENST00000475162.3:c.415+873A>T
|
|
|
ENST00000630287.2:c.*22A>T
|
ENSP00000486694.1:n.*22A>T
|
|
NM_006516.2:c.707A>T
|
NP_006507.2:p.Asp236Val
|
|
NM_006516.3:c.707A>T
|
NP_006507.2:p.Asp236Val
|
|
NM_006516.4:c.707A>T
MANE Select
|
NP_006507.2:p.Asp236Val
|
|