ENST00000433363.7:c.1012A>G
MANE Select
|
ENSP00000406220.2:p.Met338Val
|
|
ENST00000293800.10:c.961A>G
|
ENSP00000293800.6:p.Met321Val
|
|
ENST00000381074.8:c.883A>G
|
ENSP00000370464.4:p.Met295Val
|
|
ENST00000433363.6:c.1012A>G
|
ENSP00000406220.2:p.Met338Val
|
|
ENST00000572727.1:n.121A>G
|
|
|
ENST00000573648.5:c.1012A>G
|
ENSP00000459372.1:p.Met338Val
|
|
ENST00000574824.5:n.2145A>G
|
|
|
NM_001143838.2:c.1012A>G
|
NP_001137310.1:p.Met338Val
|
|
NM_001284509.1:c.961A>G
|
NP_001271438.1:p.Met321Val
|
|
NM_001284510.1:c.883A>G
|
NP_001271439.1:p.Met295Val
|
|
NM_177550.4:c.1012A>G , LRG_1020t1:c.1012A>G
|
NP_808218.1:p.Met338Val
|
|
XM_006721504.2:c.901A>G
|
XP_006721567.1:p.Met301Val
|
|
XM_011523795.1:c.1012A>G
|
XP_011522097.1:p.Met338Val
|
|
XM_011523795.3:c.1012A>G
|
XP_011522097.1:p.Met338Val
|
|
NM_001143838.3:c.1012A>G
|
NP_001137310.1:p.Met338Val
|
|
NM_001284509.2:c.961A>G
|
NP_001271438.1:p.Met321Val
|
|
NM_001284510.2:c.883A>G
|
NP_001271439.1:p.Met295Val
|
|
NM_177550.5:c.1012A>G
MANE Select
|
NP_808218.1:p.Met338Val
|
|