ENST00000399391.7:c.385A>T
|
ENSP00000382323.2:p.Arg129Ter
|
|
ENST00000399397.6:c.349A>T
MANE Select
|
ENSP00000382329.2:p.Arg117Ter
|
|
ENST00000399391.6:c.385A>T
|
ENSP00000382323.2:p.Arg129Ter
|
|
ENST00000399397.5:c.349A>T
|
ENSP00000382329.2:p.Arg117Ter
|
|
ENST00000428619.1:c.166A>T
|
ENSP00000399057.2:p.Arg56Ter
|
|
ENST00000498332.5:n.255A>T
|
|
|
NM_001277269.1:c.385A>T
|
NP_001264198.1:p.Arg129Ter
|
|
NM_001292063.1:c.349A>T
|
NP_001278992.1:p.Arg117Ter
|
|
NM_001277269.2:c.385A>T
|
NP_001264198.1:p.Arg129Ter
|
|
NM_001292063.2:c.349A>T
MANE Select
|
NP_001278992.1:p.Arg117Ter
|
|