ENST00000310546.3:c.694+13499A>G
MANE Select
|
ENSP00000311609.2:n.694+13499A>G
|
|
ENST00000310546.2:c.694+13499A>G
|
ENSP00000311609.2:n.694+13499A>G
|
|
ENST00000507895.1:n.146A>G
|
|
|
ENST00000508126.1:c.161+13499A>G
|
|
|
ENST00000508828.1:n.461A>G
|
|
|
NM_080862.2:c.694+13499A>G
|
NP_543138.1:n.694+13499A>G
|
|
XM_011513313.1:c.694+13499A>G
|
XP_011511615.1:n.694+13499A>G
|
|
XR_924215.1:n.1436A>G
|
|
|
XR_924216.1:n.1436A>G
|
|
|
XM_017007509.2:c.702A>G
|
XP_016862998.1:p.Ter234Trp
|
|
XR_924215.3:n.917A>G
|
|
|
XR_924216.3:n.917A>G
|
|
|
NM_080862.3:c.694+13499A>G
MANE Select
|
NP_543138.1:n.694+13499A>G
|
|