ENST00000225737.11:c.1925T>C
MANE Select
|
ENSP00000225737.6:p.Ile642Thr
|
|
ENST00000225737.10:c.1925T>C
|
ENSP00000225737.6:p.Ile642Thr
|
|
ENST00000395536.7:c.1751T>C
|
ENSP00000378907.3:p.Ile584Thr
|
|
ENST00000578898.1:c.352T>C
|
|
|
ENST00000583951.1:c.236T>C
|
|
|
NM_007202.3:c.1925T>C
|
NP_009133.2:p.Ile642Thr
|
|
XM_006721431.2:c.1835-3007T>C
|
XP_006721494.1:n.1835-3007T>C
|
|
XM_006721432.2:c.1751T>C
|
XP_006721495.1:p.Ile584Thr
|
|
XR_933969.1:n.1973T>C
|
|
|
XR_933970.1:n.1883-3007T>C
|
|
|
NM_001330152.1:c.1751T>C
|
NP_001317081.1:p.Ile584Thr
|
|
XR_001752418.2:n.2037T>C
|
|
|
XR_933969.3:n.1956T>C
|
|
|
NM_007202.4:c.1925T>C
MANE Select
|
NP_009133.2:p.Ile642Thr
|
|
NM_001330152.2:c.1751T>C
|
NP_001317081.1:p.Ile584Thr
|
|