ENST00000398603.6:c.337-268C>T
|
ENSP00000381604.1:n.337-268C>T
|
|
ENST00000398606.10:c.354C>T
MANE Select
|
ENSP00000381607.3:p.Asp118=
|
|
ENST00000646888.1:c.*70C>T
|
ENSP00000494477.1:n.*70C>T
|
|
ENST00000398603.5:c.337-268C>T
|
ENSP00000381604.1:n.337-268C>T
|
|
ENST00000398606.7:c.354C>T
|
ENSP00000381607.3:p.Asp118=
|
|
ENST00000467591.1:n.465C>T
|
|
|
ENST00000494593.1:n.1149C>T
|
|
|
ENST00000495996.1:c.18C>T
|
ENSP00000484686.1:p.Asp6=
|
|
ENST00000498765.5:c.417C>T
|
|
|
NM_000852.3:c.354C>T , LRG_723t1:c.354C>T
|
NP_000843.1:p.Asp118=
|
|
NM_000852.4:c.354C>T
MANE Select
|
NP_000843.1:p.Asp118=
|
|