ENST00000332826.7:c.2046C>A
MANE Select
|
ENSP00000332788.6:p.Asp682Glu
|
|
ENST00000332826.6:c.2046C>A
|
ENSP00000332788.6:p.Asp682Glu
|
|
ENST00000524802.1:n.538C>A
|
|
|
ENST00000526142.5:n.2127C>A
|
|
|
ENST00000528927.5:n.2157C>A
|
|
|
ENST00000532094.5:n.4751C>A
|
|
|
ENST00000534161.5:n.1419C>A
|
|
|
NM_001012302.2:c.2046C>A
|
NP_001012302.2:p.Asp682Glu
|
|
XM_011520046.1:c.2040C>A
|
XP_011518348.1:p.Asp680Glu
|
|
XM_011520049.1:c.1539C>A
|
XP_011518351.1:p.Asp513Glu
|
|
XM_011520053.1:c.1149C>A
|
XP_011518355.1:p.Asp383Glu
|
|
XR_428843.1:n.2102C>A
|
|
|
XR_428844.1:n.2019C>A
|
|
|
XR_930862.1:n.2213C>A
|
|
|
NM_001347882.1:c.1614C>A
|
NP_001334811.1:p.Asp538Glu
|
|
XM_011520053.2:c.1149C>A
|
XP_011518355.1:p.Asp383Glu
|
|
XR_001747846.1:n.2864C>A
|
|
|
XR_001747847.1:n.2858C>A
|
|
|
XR_001747848.1:n.2261C>A
|
|
|
XR_001747849.1:n.2868C>A
|
|
|
XR_001747850.1:n.3878C>A
|
|
|
XR_001747851.1:n.3897C>A
|
|
|
XR_001747852.1:n.2019C>A
|
|
|
XR_001747853.1:n.2960C>A
|
|
|
XR_001747854.1:n.1759C>A
|
|
|
XR_001747855.1:n.1646C>A
|
|
|
NM_001012302.3:c.2046C>A
MANE Select
|
NP_001012302.2:p.Asp682Glu
|
|
NM_001347882.2:c.1614C>A
|
NP_001334811.1:p.Asp538Glu
|
|