ENST00000477226.6:n.817T>G
|
|
|
ENST00000683013.1:n.731T>G
|
|
|
ENST00000373960.4:c.1343T>G
MANE Select
|
ENSP00000363071.3:p.Ile448Ser
|
|
ENST00000373960.3:c.1343T>G
|
ENSP00000363071.3:p.Ile448Ser
|
|
ENST00000483395.1:n.198T>G
|
|
|
NM_001927.3:c.1343T>G , LRG_380t1:c.1343T>G
|
NP_001918.3:p.Ile448Ser
|
|
NM_001927.4:c.1343T>G
MANE Select
|
NP_001918.3:p.Ile448Ser
|
|
NM_001382708.1:c.1340T>G
|
NP_001369637.1:p.Ile447Ser
|
|
NM_001382709.1:c.911T>G
|
NP_001369638.1:p.Ile304Ser
|
|
NM_001382710.1:c.1274T>G
|
NP_001369639.1:p.Ile425Ser
|
|
NM_001382711.1:c.1322T>G
|
NP_001369640.1:p.Ile441Ser
|
|
NM_001382712.1:c.1343T>G
|
NP_001369641.1:p.Ile448Ser
|
|
NM_001382713.1:c.1073T>G
|
NP_001369642.1:p.Ile358Ser
|
|