ENST00000477226.6:n.370A>T
|
|
|
ENST00000683013.1:n.284A>T
|
|
|
ENST00000373960.4:c.896A>T
MANE Select
|
ENSP00000363071.3:p.Lys299Met
|
|
ENST00000373960.3:c.896A>T
|
ENSP00000363071.3:p.Lys299Met
|
|
ENST00000477226.5:n.368A>T
|
|
|
ENST00000492726.1:n.291A>T
|
|
|
NM_001927.3:c.896A>T , LRG_380t1:c.896A>T
|
NP_001918.3:p.Lys299Met
|
|
NM_001927.4:c.896A>T
MANE Select
|
NP_001918.3:p.Lys299Met
|
|
NM_001382708.1:c.893A>T
|
NP_001369637.1:p.Lys298Met
|
|
NM_001382709.1:c.735+309A>T
|
NP_001369638.1:n.735+309A>T
|
|
NM_001382710.1:c.896A>T
|
NP_001369639.1:p.Lys299Met
|
|
NM_001382711.1:c.896A>T
|
NP_001369640.1:p.Lys299Met
|
|
NM_001382712.1:c.896A>T
|
NP_001369641.1:p.Lys299Met
|
|
NM_001382713.1:c.626A>T
|
NP_001369642.1:p.Lys209Met
|
|