ENST00000375128.5:c.677T>C
MANE Select
|
ENSP00000364270.5:p.Leu226Ser
|
|
ENST00000375128.4:c.677T>C
|
ENSP00000364270.4:p.Leu226Ser
|
|
ENST00000462523.5:c.*113T>C
|
ENSP00000433006.1:n.*113T>C
|
|
ENST00000485042.1:n.189T>C
|
|
|
NM_000380.3:c.677T>C , LRG_471t1:c.677T>C
|
NP_000371.1:p.Leu226Ser
|
|
NR_027302.1:n.1025T>C
|
|
|
XM_006717278.1:c.677T>C
|
XP_006717341.1:p.Leu226Ser
|
|
XM_011518988.1:c.677T>C
|
XP_011517290.1:p.Leu226Ser
|
|
XR_929839.1:n.1208T>C
|
|
|
NM_001354975.1:c.551T>C
|
NP_001341904.1:p.Leu184Ser
|
|
NR_149091.1:n.522T>C
|
|
|
NR_149092.1:n.688T>C
|
|
|
NR_149093.1:n.1214T>C
|
|
|
NR_149094.1:n.1108T>C
|
|
|
NM_000380.4:c.677T>C
MANE Select
|
NP_000371.1:p.Leu226Ser
|
|
NM_001354975.2:c.551T>C
|
NP_001341904.1:p.Leu184Ser
|
|
NR_027302.2:n.956T>C
|
|
|
NR_149091.2:n.453T>C
|
|
|
NR_149092.2:n.619T>C
|
|
|
NR_149093.2:n.1145T>C
|
|
|
NR_149094.2:n.1039T>C
|
|
|