ENST00000682275.1:c.1177C>G
|
ENSP00000507852.1:p.Leu393Val
|
|
ENST00000683395.1:c.1118C>G
|
|
|
ENST00000684087.1:c.1141C>G
|
ENSP00000506978.1:p.Leu381Val
|
|
ENST00000506362.2:c.892C>G
|
ENSP00000424103.2:p.Leu298Val
|
|
ENST00000673642.1:c.800C>G
|
ENSP00000501242.1:p.Ala267Gly
|
|
ENST00000673991.1:c.1177C>G
|
ENSP00000501033.1:p.Leu393Val
|
|
ENST00000226760.5:c.1141C>G
MANE Select
|
ENSP00000226760.1:p.Leu381Val
|
|
ENST00000503569.5:c.1141C>G
|
ENSP00000423337.1:p.Leu381Val
|
|
ENST00000507765.1:n.1326C>G
|
|
|
NM_001145853.1:c.1141C>G
|
NP_001139325.1:p.Leu381Val
|
|
NM_006005.3:c.1141C>G
MANE Select
|
NP_005996.2:p.Leu381Val
|
|
XM_017008586.1:c.1150C>G
|
XP_016864075.1:p.Leu384Val
|
|