ENST00000391944.8:c.2000C>A
|
ENSP00000375808.4:p.Ala667Asp
|
|
ENST00000682414.1:c.2000C>A
|
ENSP00000507019.1:p.Ala667Asp
|
|
ENST00000682508.1:n.2029C>A
|
|
|
ENST00000684218.1:c.*1258C>A
|
ENSP00000507804.1:n.*1258C>A
|
|
ENST00000684264.1:n.1556C>A
|
|
|
ENST00000684407.1:c.1877C>A
|
ENSP00000507775.1:p.Ala626Asp
|
|
ENST00000684458.1:c.*486C>A
|
ENSP00000508260.1:n.*486C>A
|
|
ENST00000684468.1:n.1712C>A
|
|
|
ENST00000391945.10:c.2000C>A
MANE Select
|
ENSP00000375809.4:p.Ala667Asp
|
|
ENST00000646507.1:n.2097C>A
|
|
|
ENST00000391941.6:c.1928C>A
|
ENSP00000375805.2:p.Ala643Asp
|
|
ENST00000391942.6:n.1171C>A
|
|
|
ENST00000391944.7:c.1766C>A
|
ENSP00000375808.3:p.Ala589Asp
|
|
ENST00000391945.8:c.2000C>A
|
ENSP00000375809.3:p.Ala667Asp
|
|
ENST00000588652.5:n.2088C>A
|
|
|
NM_000400.3:c.2000C>A , LRG_461t1:c.2000C>A
|
NP_000391.1:p.Ala667Asp
|
|
XM_011526611.1:c.1922C>A
|
XP_011524913.1:p.Ala641Asp
|
|
XM_011526611.2:c.1922C>A
|
XP_011524913.1:p.Ala641Asp
|
|
XM_017026467.1:c.1877C>A
|
XP_016881956.1:p.Ala626Asp
|
|
XR_001753633.2:n.2047C>A
|
|
|
XR_001753634.2:n.1983C>A
|
|
|
NM_000400.4:c.2000C>A
MANE Select
|
NP_000391.1:p.Ala667Asp
|
|