ENST00000477226.6:n.246C>T
|
|
|
ENST00000683013.1:n.160C>T
|
|
|
ENST00000373960.4:c.772C>T
MANE Select
|
ENSP00000363071.3:p.Gln258Ter
|
|
ENST00000373960.3:c.772C>T
|
ENSP00000363071.3:p.Gln258Ter
|
|
ENST00000477226.5:n.244C>T
|
|
|
ENST00000492726.1:n.167C>T
|
|
|
NM_001927.3:c.772C>T , LRG_380t1:c.772C>T
|
NP_001918.3:p.Gln258Ter
|
|
NM_001927.4:c.772C>T
MANE Select
|
NP_001918.3:p.Gln258Ter
|
|
NM_001382708.1:c.769C>T
|
NP_001369637.1:p.Gln257Ter
|
|
NM_001382709.1:c.735+185C>T
|
NP_001369638.1:n.735+185C>T
|
|
NM_001382710.1:c.772C>T
|
NP_001369639.1:p.Gln258Ter
|
|
NM_001382711.1:c.772C>T
|
NP_001369640.1:p.Gln258Ter
|
|
NM_001382712.1:c.772C>T
|
NP_001369641.1:p.Gln258Ter
|
|
NM_001382713.1:c.502C>T
|
NP_001369642.1:p.Gln168Ter
|
|