ENST00000426263.10:c.944T>C
MANE Select
|
ENSP00000416293.2:p.Ile315Thr
|
|
ENST00000674545.1:n.262T>C
|
|
|
ENST00000674765.1:c.944T>C
|
ENSP00000501811.1:p.Ile315Thr
|
|
ENST00000675112.1:n.1245T>C
|
|
|
ENST00000676254.1:n.1393T>C
|
|
|
ENST00000426263.7:c.944T>C
|
ENSP00000416293.2:p.Ile315Thr
|
|
ENST00000439722.2:c.823T>C
|
ENSP00000395521.2:n.823T>C
|
|
ENST00000475162.3:c.415+1388T>C
|
|
|
ENST00000630287.2:c.*259T>C
|
ENSP00000486694.1:n.*259T>C
|
|
NM_006516.2:c.944T>C
|
NP_006507.2:p.Ile315Thr
|
|
NM_006516.3:c.944T>C
|
NP_006507.2:p.Ile315Thr
|
|
NM_006516.4:c.944T>C
MANE Select
|
NP_006507.2:p.Ile315Thr
|
|