ENST00000454220.7:c.766G>T
|
ENSP00000391905.3:p.Glu256Ter
|
|
ENST00000703395.1:c.109G>T
|
ENSP00000515286.1:p.Glu37Ter
|
|
ENST00000703396.1:n.590G>T
|
|
|
ENST00000703397.1:c.109G>T
|
ENSP00000515287.1:p.Glu37Ter
|
|
ENST00000703398.1:c.688G>T
|
ENSP00000515288.1:p.Glu230Ter
|
|
ENST00000703421.1:n.799G>T
|
|
|
ENST00000703422.1:c.622G>T
|
ENSP00000515292.1:p.Glu208Ter
|
|
ENST00000703423.1:c.109G>T
|
ENSP00000515293.1:p.Glu37Ter
|
|
ENST00000322088.11:c.646G>T
MANE Select
|
ENSP00000324804.6:p.Glu216Ter
|
|
ENST00000322088.10:c.646G>T
|
ENSP00000324804.6:p.Glu216Ter
|
|
ENST00000454220.6:c.766G>T
|
ENSP00000391905.2:p.Glu256Ter
|
|
ENST00000462047.1:n.337G>T
|
|
|
ENST00000462990.5:c.109G>T
|
ENSP00000470504.1:p.Glu37Ter
|
|
NM_014225.5:c.646G>T
|
NP_055040.2:p.Glu216Ter
|
|
NR_033500.1:n.840G>T
|
|
|
NM_001363656.1:c.109G>T
|
NP_001350585.1:p.Glu37Ter
|
|
NM_014225.6:c.646G>T
MANE Select
|
NP_055040.2:p.Glu216Ter
|
|
NM_001363656.2:c.109G>T
|
NP_001350585.1:p.Glu37Ter
|
|
NR_033500.2:n.590G>T
|
|
|