ENST00000205402.10:c.1006A>T
MANE Select
|
ENSP00000205402.3:p.Arg336Ter
|
|
ENST00000205402.9:c.1006A>T
|
ENSP00000205402.3:p.Arg336Ter
|
|
ENST00000415325.5:c.*680A>T
|
ENSP00000402593.1:n.*680A>T
|
|
ENST00000417551.5:c.1006A>T
|
ENSP00000390667.1:p.Arg336Ter
|
|
ENST00000437604.6:c.862A>T
|
ENSP00000387542.2:p.Arg288Ter
|
|
ENST00000440410.5:c.937A>T
|
ENSP00000417016.1:p.Arg313Ter
|
|
NM_000108.4:c.1006A>T
|
NP_000099.2:p.Arg336Ter
|
|
NM_001289750.1:c.709A>T
|
NP_001276679.1:p.Arg237Ter
|
|
NM_001289751.1:c.937A>T
|
NP_001276680.1:p.Arg313Ter
|
|
NM_001289752.1:c.862A>T
|
NP_001276681.1:p.Arg288Ter
|
|
NM_000108.5:c.1006A>T
MANE Select
|
NP_000099.2:p.Arg336Ter
|
|