ENST00000426263.10:c.575T>C
MANE Select
|
ENSP00000416293.2:p.Ile192Thr
|
|
ENST00000674765.1:c.575T>C
|
ENSP00000501811.1:p.Ile192Thr
|
|
ENST00000675112.1:n.598T>C
|
|
|
ENST00000676254.1:n.1024T>C
|
|
|
ENST00000426263.7:c.575T>C
|
ENSP00000416293.2:p.Ile192Thr
|
|
ENST00000439722.2:c.454T>C
|
ENSP00000395521.2:n.454T>C
|
|
ENST00000475162.3:c.415+649T>C
|
|
|
ENST00000630287.2:c.517-197T>C
|
ENSP00000486694.1:n.517-197T>C
|
|
NM_006516.2:c.575T>C
|
NP_006507.2:p.Ile192Thr
|
|
NM_006516.3:c.575T>C
|
NP_006507.2:p.Ile192Thr
|
|
NM_006516.4:c.575T>C
MANE Select
|
NP_006507.2:p.Ile192Thr
|
|