ENST00000433363.7:c.380G>T
MANE Select
|
ENSP00000406220.2:p.Gly127Val
|
|
ENST00000293800.10:c.369-40G>T
|
ENSP00000293800.6:n.369-40G>T
|
|
ENST00000381074.8:c.251G>T
|
ENSP00000370464.4:p.Gly84Val
|
|
ENST00000433363.6:c.380G>T
|
ENSP00000406220.2:p.Gly127Val
|
|
ENST00000572094.1:c.*130G>T
|
ENSP00000461495.1:n.*130G>T
|
|
ENST00000572352.5:c.269G>T
|
ENSP00000461622.1:p.Gly90Val
|
|
ENST00000573648.5:c.380G>T
|
ENSP00000459372.1:p.Gly127Val
|
|
ENST00000574824.5:n.1513G>T
|
|
|
ENST00000575230.1:c.*226G>T
|
ENSP00000460903.1:n.*226G>T
|
|
ENST00000576323.1:n.410G>T
|
|
|
NM_001143838.2:c.380G>T
|
NP_001137310.1:p.Gly127Val
|
|
NM_001284509.1:c.369-40G>T
|
NP_001271438.1:n.369-40G>T
|
|
NM_001284510.1:c.251G>T
|
NP_001271439.1:p.Gly84Val
|
|
NM_177550.4:c.380G>T , LRG_1020t1:c.380G>T
|
NP_808218.1:p.Gly127Val
|
|
XM_006721504.2:c.269G>T
|
XP_006721567.1:p.Gly90Val
|
|
XM_011523795.1:c.380G>T
|
XP_011522097.1:p.Gly127Val
|
|
XM_011523795.3:c.380G>T
|
XP_011522097.1:p.Gly127Val
|
|
NM_001143838.3:c.380G>T
|
NP_001137310.1:p.Gly127Val
|
|
NM_001284509.2:c.369-40G>T
|
NP_001271438.1:n.369-40G>T
|
|
NM_001284510.2:c.251G>T
|
NP_001271439.1:p.Gly84Val
|
|
NM_177550.5:c.380G>T
MANE Select
|
NP_808218.1:p.Gly127Val
|
|