ENST00000348974.5:c.1806A>C
|
ENSP00000330021.7:p.Arg602Ser
|
|
ENST00000394236.9:c.1806A>C
MANE Select
|
ENSP00000377783.3:p.Arg602Ser
|
|
ENST00000407433.6:c.1761A>C
|
ENSP00000385794.2:p.Arg587Ser
|
|
ENST00000647936.1:c.1644+2133A>C
|
ENSP00000496822.1:n.1644+2133A>C
|
|
ENST00000648381.1:n.1974A>C
|
|
|
ENST00000648853.1:c.1764A>C
|
ENSP00000497262.1:p.Arg588Ser
|
|
ENST00000649585.1:c.749A>C
|
ENSP00000498163.1:n.749A>C
|
|
ENST00000650591.1:c.1902A>C
|
ENSP00000497376.1:p.Arg634Ser
|
|
ENST00000394236.7:c.1806A>C
|
ENSP00000377783.3:p.Arg602Ser
|
|
ENST00000407433.5:c.1413A>C
|
ENSP00000385794.1:p.Arg471Ser
|
|
NM_000313.3:c.1806A>C , LRG_572t1:c.1806A>C
|
NP_000304.2:p.Arg602Ser
|
|
NM_001314077.1:c.1902A>C , LRG_572t2:c.1902A>C
|
NP_001301006.1:p.Arg634Ser
|
|
NM_000313.4:c.1806A>C
MANE Select
|
NP_000304.2:p.Arg602Ser
|
|
NM_001314077.2:c.1902A>C
|
NP_001301006.1:p.Arg634Ser
|
|