ENST00000297289.9:c.373G>T
|
ENSP00000516619.1:p.Glu125Ter
|
|
ENST00000418964.2:c.1471G>T
|
ENSP00000389424.2:p.Glu491Ter
|
|
ENST00000706906.1:c.1420G>T
|
ENSP00000516618.1:p.Glu474Ter
|
|
ENST00000308192.14:c.1420G>T
MANE Select
|
ENSP00000308938.9:p.Glu474Ter
|
|
ENST00000297289.8:n.418G>T
|
|
|
ENST00000308192.13:c.1420G>T
|
ENSP00000308938.9:p.Glu474Ter
|
|
ENST00000493435.1:n.475G>T
|
|
|
NM_000301.3:c.1420G>T , LRG_571t1:c.1420G>T
|
NP_000292.1:p.Glu474Ter
|
|
NM_000301.4:c.1420G>T
|
NP_000292.1:p.Glu474Ter
|
|
NM_000301.5:c.1420G>T
MANE Select
|
NP_000292.1:p.Glu474Ter
|
|