ENST00000398603.6:c.350A>T
|
ENSP00000381604.1:p.Asp117Val
|
|
ENST00000398606.10:c.458A>T
MANE Select
|
ENSP00000381607.3:p.Asp153Val
|
|
ENST00000646888.1:c.*174A>T
|
ENSP00000494477.1:n.*174A>T
|
|
ENST00000398603.5:c.350A>T
|
ENSP00000381604.1:p.Asp117Val
|
|
ENST00000398606.7:c.458A>T
|
ENSP00000381607.3:p.Asp153Val
|
|
ENST00000467591.1:n.569A>T
|
|
|
ENST00000494593.1:n.1430A>T
|
|
|
ENST00000495996.1:c.184A>T
|
ENSP00000484686.1:p.Thr62Ser
|
|
ENST00000498765.5:c.521A>T
|
|
|
NM_000852.3:c.458A>T , LRG_723t1:c.458A>T
|
NP_000843.1:p.Asp153Val
|
|
NM_000852.4:c.458A>T
MANE Select
|
NP_000843.1:p.Asp153Val
|
|