ENST00000477226.6:n.765A>G
|
|
|
ENST00000683013.1:n.679A>G
|
|
|
ENST00000373960.4:c.1291A>G
MANE Select
|
ENSP00000363071.3:p.Thr431Ala
|
|
ENST00000373960.3:c.1291A>G
|
ENSP00000363071.3:p.Thr431Ala
|
|
ENST00000483395.1:n.146A>G
|
|
|
NM_001927.3:c.1291A>G , LRG_380t1:c.1291A>G
|
NP_001918.3:p.Thr431Ala
|
|
NM_001927.4:c.1291A>G
MANE Select
|
NP_001918.3:p.Thr431Ala
|
|
NM_001382708.1:c.1288A>G
|
NP_001369637.1:p.Thr430Ala
|
|
NM_001382709.1:c.859A>G
|
NP_001369638.1:p.Thr287Ala
|
|
NM_001382710.1:c.1222A>G
|
NP_001369639.1:p.Thr408Ala
|
|
NM_001382711.1:c.1270A>G
|
NP_001369640.1:p.Thr424Ala
|
|
NM_001382712.1:c.1291A>G
|
NP_001369641.1:p.Thr431Ala
|
|
NM_001382713.1:c.1021A>G
|
NP_001369642.1:p.Thr341Ala
|
|