ENST00000673913.2:c.*292A>T
|
ENSP00000501161.2:n.*292A>T
|
|
ENST00000710286.1:c.2309A>T
|
ENSP00000518176.1:p.Asp770Val
|
|
ENST00000673903.1:c.1577A>T
|
ENSP00000501257.1:p.Asp526Val
|
|
ENST00000673913.1:c.802A>T
|
ENSP00000501161.1:n.802A>T
|
|
ENST00000302118.5:c.1952A>T
MANE Select
|
ENSP00000303208.5:p.Asp651Val
|
|
ENST00000490692.1:n.2498A>T
|
|
|
NM_174936.3:c.1952A>T , LRG_275t1:c.1952A>T
|
NP_777596.2:p.Asp651Val
|
|
NR_110451.1:n.1559A>T
|
|
|
XM_011541193.1:c.1073A>T
|
XP_011539495.1:p.Asp358Val
|
|
NM_174936.4:c.1952A>T
MANE Select
|
NP_777596.2:p.Asp651Val
|
|
NR_110451.2:n.1559A>T
|
|
|