ENST00000684241.1:n.1632C>G
|
|
|
ENST00000262186.10:c.799C>G
MANE Select
|
ENSP00000262186.5:p.Leu267Val
|
|
ENST00000262186.9:c.799C>G
|
ENSP00000262186.5:p.Leu267Val
|
|
ENST00000430723.4:c.451C>G
|
ENSP00000387657.4:p.Leu151Val
|
|
ENST00000532957.5:n.1022C>G
|
|
|
NM_000238.3:c.799C>G , LRG_288t1:c.799C>G
|
NP_000229.1:p.Leu267Val
|
|
NM_172056.2:c.799C>G , LRG_288t2:c.799C>G
|
NP_742053.1:p.Leu267Val
|
|
XM_011516185.1:c.499C>G
|
XP_011514487.1:p.Leu167Val
|
|
XM_011516186.1:c.799C>G
|
XP_011514488.1:p.Leu267Val
|
|
XM_011516185.2:c.499C>G
|
XP_011514487.1:p.Leu167Val
|
|
XM_011516186.3:c.799C>G
|
XP_011514488.1:p.Leu267Val
|
|
XM_017012195.1:c.649C>G
|
XP_016867684.1:p.Leu217Val
|
|
XM_017012196.1:c.622C>G
|
XP_016867685.1:p.Leu208Val
|
|
NM_000238.4:c.799C>G
MANE Select
|
NP_000229.1:p.Leu267Val
|
|