ENST00000617979.5:c.348G>T
MANE Select
|
ENSP00000483375.1:p.Leu116=
|
|
ENST00000374497.7:c.348G>T
|
ENSP00000363621.3:p.Leu116=
|
|
ENST00000418277.5:c.156G>T
|
ENSP00000414719.1:p.Leu52=
|
|
ENST00000425913.5:c.348G>T
|
ENSP00000393359.1:p.Leu116=
|
|
ENST00000429356.5:c.156G>T
|
ENSP00000398585.1:p.Leu52=
|
|
ENST00000445705.1:c.348G>T
|
ENSP00000398257.1:p.Leu116=
|
|
ENST00000459934.5:n.466G>T
|
|
|
ENST00000467493.5:n.808G>T
|
|
|
ENST00000470949.5:n.293G>T
|
|
|
ENST00000481736.5:n.752G>T
|
|
|
ENST00000486382.1:n.449G>T
|
|
|
ENST00000617979.4:c.348G>T
|
ENSP00000483375.1:p.Leu116=
|
|
NM_000403.3:c.348G>T
|
NP_000394.2:p.Leu116=
|
|
NM_001008216.1:c.348G>T
|
NP_001008217.1:p.Leu116=
|
|
NM_001127621.1:c.348G>T
|
NP_001121093.1:p.Leu116=
|
|
NM_001008216.2:c.348G>T
MANE Select
|
NP_001008217.1:p.Leu116=
|
|
NM_000403.4:c.348G>T
|
NP_000394.2:p.Leu116=
|
|
NM_001127621.2:c.348G>T
|
NP_001121093.1:p.Leu116=
|
|