ENST00000398603.6:c.447T>A
|
ENSP00000381604.1:p.Ser149Arg
|
|
ENST00000398606.10:c.555T>A
MANE Select
|
ENSP00000381607.3:p.Ser185Arg
|
|
ENST00000646888.1:c.*271T>A
|
ENSP00000494477.1:n.*271T>A
|
|
ENST00000398603.5:c.447T>A
|
ENSP00000381604.1:p.Ser149Arg
|
|
ENST00000398606.7:c.555T>A
|
ENSP00000381607.3:p.Ser185Arg
|
|
ENST00000467591.1:n.666T>A
|
|
|
ENST00000494593.1:n.1527T>A
|
|
|
ENST00000498765.5:c.618T>A
|
|
|
NM_000852.3:c.555T>A , LRG_723t1:c.555T>A
|
NP_000843.1:p.Ser185Arg
|
|
NM_000852.4:c.555T>A
MANE Select
|
NP_000843.1:p.Ser185Arg
|
|