ENST00000405460.9:c.16256T>A
MANE Select
|
ENSP00000384582.2:p.Leu5419His
|
|
ENST00000425867.3:c.5210T>A
|
ENSP00000392618.3:p.Leu1737His
|
|
ENST00000638510.1:n.3523T>A
|
|
|
ENST00000639431.1:c.265+147275T>A
|
ENSP00000491057.1:n.265+147275T>A
|
|
ENST00000640061.1:n.128+1302T>A
|
|
|
ENST00000640407.1:c.2666T>A
|
ENSP00000491425.1:p.Leu889His
|
|
ENST00000405460.6:c.16256T>A
|
ENSP00000384582.2:p.Leu5419His
|
|
ENST00000425867.2:c.3239T>A
|
ENSP00000392618.2:p.Leu1080His
|
|
NM_032119.3:c.16256T>A
|
NP_115495.3:p.Leu5419His
|
|
NR_003149.1:n.16269T>A
|
|
|
XM_011543675.1:c.16253T>A
|
XP_011541977.1:p.Leu5418His
|
|
XM_011543676.1:c.16175T>A
|
XP_011541978.1:p.Leu5392His
|
|
XM_011543677.1:c.13559T>A
|
XP_011541979.1:p.Leu4520His
|
|
NM_032119.4:c.16256T>A
MANE Select
|
NP_115495.3:p.Leu5419His
|
|
XM_017009963.2:c.16277T>A
|
XP_016865452.1:p.Leu5426His
|
|
XM_017009964.2:c.16274T>A
|
XP_016865453.1:p.Leu5425His
|
|
XM_017009965.1:c.16274T>A
|
XP_016865454.1:p.Leu5425His
|
|
XM_017009966.2:c.16196T>A
|
XP_016865455.1:p.Leu5399His
|
|
XM_017009967.1:c.16181T>A
|
XP_016865456.1:p.Leu5394His
|
|
XM_017009968.2:c.16097T>A
|
XP_016865457.1:p.Leu5366His
|
|
XM_017009969.2:c.16277T>A
|
XP_016865458.1:p.Leu5426His
|
|
XM_017009972.1:c.9395T>A
|
XP_016865461.1:p.Leu3132His
|
|
XM_017009973.1:c.9374T>A
|
XP_016865462.1:p.Leu3125His
|
|
NR_003149.2:n.16272T>A
|
|
|