ENST00000281182.9:c.1194A>C
MANE Select
|
ENSP00000281182.5:p.Glu398Asp
|
|
ENST00000281182.8:c.1194A>C
|
ENSP00000281182.4:p.Glu398Asp
|
|
ENST00000374752.6:c.813A>C
|
ENSP00000363884.4:p.Glu271Asp
|
|
ENST00000524502.2:n.194A>C
|
|
|
ENST00000526026.5:c.*883A>C
|
ENSP00000431532.1:n.*883A>C
|
|
ENST00000531338.5:n.1438A>C
|
|
|
ENST00000533387.5:n.2253A>C
|
|
|
NM_014384.2:c.1194A>C , LRG_448t1:c.1194A>C
|
NP_055199.1:p.Glu398Asp
|
|
XM_005271501.2:c.1194A>C
|
XP_005271558.1:p.Glu398Asp
|
|
XM_011542750.1:c.1194A>C
|
XP_011541052.1:p.Glu398Asp
|
|
XR_947819.1:n.1258A>C
|
|
|
XR_947820.1:n.1646A>C
|
|
|
XR_947822.1:n.1088A>C
|
|
|
XR_947823.1:n.1244A>C
|
|
|
XM_005271505.4:c.*1459A>C
|
XP_005271562.1:n.*1459A>C
|
|
XM_011542750.3:c.1194A>C
|
XP_011541052.1:p.Glu398Asp
|
|
XM_017017542.2:c.1194A>C
|
XP_016873031.1:p.Glu398Asp
|
|
XM_017017543.2:c.1194A>C
|
XP_016873032.1:p.Glu398Asp
|
|
XM_017017544.2:c.*163A>C
|
XP_016873033.1:n.*163A>C
|
|
XM_017017545.2:c.*406A>C
|
XP_016873034.1:n.*406A>C
|
|
XM_017017546.2:c.900A>C
|
XP_016873035.1:p.Glu300Asp
|
|
XM_017017547.2:c.900A>C
|
XP_016873036.1:p.Glu300Asp
|
|
XM_017017548.2:c.*1830A>C
|
XP_016873037.1:n.*1830A>C
|
|
XM_017017549.2:c.*1604A>C
|
XP_016873038.1:n.*1604A>C
|
|
XM_024448437.1:c.*341A>C
|
XP_024304205.1:n.*341A>C
|
|
XM_024448438.1:c.813A>C
|
XP_024304206.1:p.Glu271Asp
|
|
NM_014384.3:c.1194A>C
MANE Select
|
NP_055199.1:p.Glu398Asp
|
|