ENST00000272602.7:c.694A>G
MANE Select
|
ENSP00000272602.2:p.Met232Val
|
|
ENST00000272602.6:c.694A>G
|
ENSP00000272602.2:p.Met232Val
|
|
ENST00000393504.5:c.694A>G
|
ENSP00000377140.1:p.Met232Val
|
|
ENST00000409937.1:c.706A>G
|
ENSP00000386761.1:p.Met236Val
|
|
ENST00000436404.6:c.640A>G
|
ENSP00000410070.2:p.Met214Val
|
|
NM_001079878.1:c.640A>G
|
NP_001073347.1:p.Met214Val
|
|
NM_001298.2:c.694A>G
|
NP_001289.1:p.Met232Val
|
|
XM_006712243.2:c.805A>G
|
XP_006712306.1:p.Met269Val
|
|
XM_011510554.1:c.859A>G
|
XP_011508856.1:p.Met287Val
|
|
XM_011510554.2:c.859A>G
|
XP_011508856.1:p.Met287Val
|
|
NM_001079878.2:c.640A>G
|
NP_001073347.1:p.Met214Val
|
|
NM_001298.3:c.694A>G
MANE Select
|
NP_001289.1:p.Met232Val
|
|