ENST00000398603.6:c.409G>T
|
ENSP00000381604.1:p.Ala137Ser
|
|
ENST00000398606.10:c.517G>T
MANE Select
|
ENSP00000381607.3:p.Ala173Ser
|
|
ENST00000646888.1:c.*233G>T
|
ENSP00000494477.1:n.*233G>T
|
|
ENST00000398603.5:c.409G>T
|
ENSP00000381604.1:p.Ala137Ser
|
|
ENST00000398606.7:c.517G>T
|
ENSP00000381607.3:p.Ala173Ser
|
|
ENST00000467591.1:n.628G>T
|
|
|
ENST00000494593.1:n.1489G>T
|
|
|
ENST00000498765.5:c.580G>T
|
|
|
NM_000852.3:c.517G>T , LRG_723t1:c.517G>T
|
NP_000843.1:p.Ala173Ser
|
|
NM_000852.4:c.517G>T
MANE Select
|
NP_000843.1:p.Ala173Ser
|
|