ENST00000375128.5:c.685G>C
MANE Select
|
ENSP00000364270.5:p.Ala229Pro
|
|
ENST00000375128.4:c.685G>C
|
ENSP00000364270.4:p.Ala229Pro
|
|
ENST00000462523.5:c.*121G>C
|
ENSP00000433006.1:n.*121G>C
|
|
ENST00000485042.1:n.197G>C
|
|
|
NM_000380.3:c.685G>C , LRG_471t1:c.685G>C
|
NP_000371.1:p.Ala229Pro
|
|
NR_027302.1:n.1033G>C
|
|
|
XM_006717278.1:c.685G>C
|
XP_006717341.1:p.Ala229Pro
|
|
XM_011518988.1:c.685G>C
|
XP_011517290.1:p.Ala229Pro
|
|
XR_929839.1:n.1216G>C
|
|
|
NM_001354975.1:c.559G>C
|
NP_001341904.1:p.Ala187Pro
|
|
NR_149091.1:n.530G>C
|
|
|
NR_149092.1:n.696G>C
|
|
|
NR_149093.1:n.1222G>C
|
|
|
NR_149094.1:n.1116G>C
|
|
|
NM_000380.4:c.685G>C
MANE Select
|
NP_000371.1:p.Ala229Pro
|
|
NM_001354975.2:c.559G>C
|
NP_001341904.1:p.Ala187Pro
|
|
NR_027302.2:n.964G>C
|
|
|
NR_149091.2:n.461G>C
|
|
|
NR_149092.2:n.627G>C
|
|
|
NR_149093.2:n.1153G>C
|
|
|
NR_149094.2:n.1047G>C
|
|
|