ENST00000433363.7:c.503C>T
MANE Select
|
ENSP00000406220.2:p.Ala168Val
|
|
ENST00000293800.10:c.452C>T
|
ENSP00000293800.6:p.Ala151Val
|
|
ENST00000381074.8:c.374C>T
|
ENSP00000370464.4:p.Ala125Val
|
|
ENST00000433363.6:c.503C>T
|
ENSP00000406220.2:p.Ala168Val
|
|
ENST00000572094.1:c.*253C>T
|
ENSP00000461495.1:n.*253C>T
|
|
ENST00000572352.5:c.392C>T
|
ENSP00000461622.1:p.Ala131Val
|
|
ENST00000573648.5:c.503C>T
|
ENSP00000459372.1:p.Ala168Val
|
|
ENST00000574824.5:n.1636C>T
|
|
|
ENST00000576323.1:n.533C>T
|
|
|
NM_001143838.2:c.503C>T
|
NP_001137310.1:p.Ala168Val
|
|
NM_001284509.1:c.452C>T
|
NP_001271438.1:p.Ala151Val
|
|
NM_001284510.1:c.374C>T
|
NP_001271439.1:p.Ala125Val
|
|
NM_177550.4:c.503C>T , LRG_1020t1:c.503C>T
|
NP_808218.1:p.Ala168Val
|
|
XM_006721504.2:c.392C>T
|
XP_006721567.1:p.Ala131Val
|
|
XM_011523795.1:c.503C>T
|
XP_011522097.1:p.Ala168Val
|
|
XM_011523795.3:c.503C>T
|
XP_011522097.1:p.Ala168Val
|
|
NM_001143838.3:c.503C>T
|
NP_001137310.1:p.Ala168Val
|
|
NM_001284509.2:c.452C>T
|
NP_001271438.1:p.Ala151Val
|
|
NM_001284510.2:c.374C>T
|
NP_001271439.1:p.Ala125Val
|
|
NM_177550.5:c.503C>T
MANE Select
|
NP_808218.1:p.Ala168Val
|
|