ENST00000398603.6:c.337-269A>T
|
ENSP00000381604.1:n.337-269A>T
|
|
ENST00000398606.10:c.353A>T
MANE Select
|
ENSP00000381607.3:p.Asp118Val
|
|
ENST00000646888.1:c.*69A>T
|
ENSP00000494477.1:n.*69A>T
|
|
ENST00000398603.5:c.337-269A>T
|
ENSP00000381604.1:n.337-269A>T
|
|
ENST00000398606.7:c.353A>T
|
ENSP00000381607.3:p.Asp118Val
|
|
ENST00000467591.1:n.464A>T
|
|
|
ENST00000494593.1:n.1148A>T
|
|
|
ENST00000495996.1:c.17A>T
|
ENSP00000484686.1:p.Asp6Val
|
|
ENST00000498765.5:c.416A>T
|
|
|
NM_000852.3:c.353A>T , LRG_723t1:c.353A>T
|
NP_000843.1:p.Asp118Val
|
|
NM_000852.4:c.353A>T
MANE Select
|
NP_000843.1:p.Asp118Val
|
|