ENST00000237596.7:c.1112A>T
MANE Select
|
ENSP00000237596.2:p.Glu371Val
|
|
ENST00000237596.6:c.1112A>T
|
ENSP00000237596.2:p.Glu371Val
|
|
ENST00000506367.1:n.559A>T
|
|
|
NM_000297.3:c.1112A>T
|
NP_000288.1:p.Glu371Val
|
|
XM_011532028.1:c.1095-3392A>T
|
XP_011530330.1:n.1095-3392A>T
|
|
XM_011532029.1:c.392A>T
|
XP_011530331.1:p.Glu131Val
|
|
XM_011532030.1:c.272A>T
|
XP_011530332.1:p.Glu91Val
|
|
XR_244632.2:n.1207A>T
|
|
|
NR_156488.1:n.1199A>T
|
|
|
XM_011532028.2:c.1095-3392A>T
|
XP_011530330.1:n.1095-3392A>T
|
|
XM_011532030.2:c.272A>T
|
XP_011530332.1:p.Glu91Val
|
|
NM_000297.4:c.1112A>T
MANE Select
|
NP_000288.1:p.Glu371Val
|
|
NR_156488.2:n.1211A>T
|
|
|