ENST00000391944.8:c.2109T>G
|
ENSP00000375808.4:p.Asp703Glu
|
|
ENST00000682414.1:c.2109T>G
|
ENSP00000507019.1:p.Asp703Glu
|
|
ENST00000682508.1:n.2138T>G
|
|
|
ENST00000684218.1:c.*1367T>G
|
ENSP00000507804.1:n.*1367T>G
|
|
ENST00000684264.1:n.1665T>G
|
|
|
ENST00000684407.1:c.1986T>G
|
ENSP00000507775.1:p.Asp662Glu
|
|
ENST00000684458.1:c.*595T>G
|
ENSP00000508260.1:n.*595T>G
|
|
ENST00000684468.1:n.1821T>G
|
|
|
ENST00000391945.10:c.2109T>G
MANE Select
|
ENSP00000375809.4:p.Asp703Glu
|
|
ENST00000646507.1:n.2206T>G
|
|
|
ENST00000391941.6:c.2037T>G
|
ENSP00000375805.2:p.Asp679Glu
|
|
ENST00000391942.6:n.1280T>G
|
|
|
ENST00000391944.7:c.1875T>G
|
ENSP00000375808.3:p.Asp625Glu
|
|
ENST00000391945.8:c.2109T>G
|
ENSP00000375809.3:p.Asp703Glu
|
|
ENST00000588652.5:n.2197T>G
|
|
|
NM_000400.3:c.2109T>G , LRG_461t1:c.2109T>G
|
NP_000391.1:p.Asp703Glu
|
|
XM_011526611.1:c.2031T>G
|
XP_011524913.1:p.Asp677Glu
|
|
XM_011526611.2:c.2031T>G
|
XP_011524913.1:p.Asp677Glu
|
|
XM_017026467.1:c.1986T>G
|
XP_016881956.1:p.Asp662Glu
|
|
XR_001753633.2:n.2156T>G
|
|
|
XR_001753634.2:n.2092T>G
|
|
|
NM_000400.4:c.2109T>G
MANE Select
|
NP_000391.1:p.Asp703Glu
|
|