ENST00000262407.6:c.715C>A
MANE Select
|
ENSP00000262407.5:p.Arg239Ser
|
|
ENST00000648408.1:c.146C>A
|
|
|
ENST00000262407.5:c.715C>A
|
ENSP00000262407.5:p.Arg239Ser
|
|
ENST00000589645.5:n.166C>A
|
|
|
ENST00000591990.5:n.77C>A
|
|
|
ENST00000592075.5:n.84C>A
|
|
|
ENST00000592226.5:n.39+132C>A
|
|
|
ENST00000592253.5:n.223C>A
|
|
|
ENST00000592944.1:n.397C>A
|
|
|
NM_000419.3:c.715C>A , LRG_479t1:c.715C>A
|
NP_000410.2:p.Arg239Ser
|
|
XM_011524749.1:c.715C>A
|
XP_011523051.1:p.Arg239Ser
|
|
XM_011524750.1:c.715C>A
|
XP_011523052.1:p.Arg239Ser
|
|
NM_000419.4:c.715C>A
|
NP_000410.2:p.Arg239Ser
|
|
NM_000419.5:c.715C>A
MANE Select
|
NP_000410.2:p.Arg239Ser
|
|