ENST00000231948.9:c.937G>C
MANE Select
|
ENSP00000231948.4:p.Asp313His
|
|
ENST00000639284.1:c.937G>C
|
ENSP00000491442.1:p.Asp313His
|
|
ENST00000231948.8:c.937G>C
|
ENSP00000231948.4:p.Asp313His
|
|
ENST00000424814.5:c.924G>C
|
|
|
ENST00000432408.6:c.934G>C
|
ENSP00000412499.2:p.Asp312His
|
|
ENST00000459840.5:n.326G>C
|
|
|
ENST00000488263.5:n.2811G>C
|
|
|
ENST00000491834.5:n.2892G>C
|
|
|
ENST00000498442.1:n.219G>C
|
|
|
NM_001173482.1:c.934G>C
|
NP_001166953.1:p.Asp312His
|
|
NM_016302.3:c.937G>C
|
NP_057386.2:p.Asp313His
|
|
XM_005265202.2:c.748G>C
|
XP_005265259.1:p.Asp250His
|
|
XM_011533791.1:c.937G>C
|
XP_011532093.1:p.Asp313His
|
|
XM_011533792.1:c.836-486G>C
|
XP_011532094.1:n.836-486G>C
|
|
XM_011533793.1:c.445G>C
|
XP_011532095.1:p.Asp149His
|
|
XM_011533794.1:c.445G>C
|
XP_011532096.1:p.Asp149His
|
|
XR_940448.1:n.853-486G>C
|
|
|
XM_005265202.4:c.748G>C
|
XP_005265259.1:p.Asp250His
|
|
XM_011533791.3:c.937G>C
|
XP_011532093.1:p.Asp313His
|
|
XM_011533793.2:c.445G>C
|
XP_011532095.1:p.Asp149His
|
|
XM_011533794.2:c.445G>C
|
XP_011532096.1:p.Asp149His
|
|
XM_024453551.1:c.836-486G>C
|
XP_024309319.1:n.836-486G>C
|
|
XR_940448.3:n.850-486G>C
|
|
|
NM_016302.4:c.937G>C
MANE Select
|
NP_057386.2:p.Asp313His
|
|