ENST00000405460.9:c.10859C>A
MANE Select
|
ENSP00000384582.2:p.Ser3620Tyr
|
|
ENST00000639431.1:c.265+69471C>A
|
ENSP00000491057.1:n.265+69471C>A
|
|
ENST00000640374.1:n.4003C>A
|
|
|
ENST00000640464.1:n.1278C>A
|
|
|
ENST00000405460.6:c.10859C>A
|
ENSP00000384582.2:p.Ser3620Tyr
|
|
ENST00000509621.1:c.3556C>A
|
|
|
NM_032119.3:c.10859C>A
|
NP_115495.3:p.Ser3620Tyr
|
|
NR_003149.1:n.10872C>A
|
|
|
XM_011543675.1:c.10856C>A
|
XP_011541977.1:p.Ser3619Tyr
|
|
XM_011543676.1:c.10778C>A
|
XP_011541978.1:p.Ser3593Tyr
|
|
XM_011543677.1:c.8162C>A
|
XP_011541979.1:p.Ser2721Tyr
|
|
XM_011543678.1:c.10859C>A
|
XP_011541980.1:p.Ser3620Tyr
|
|
XM_011543679.1:c.*81C>A
|
XP_011541981.1:n.*81C>A
|
|
NM_032119.4:c.10859C>A
MANE Select
|
NP_115495.3:p.Ser3620Tyr
|
|
XM_017009963.2:c.10880C>A
|
XP_016865452.1:p.Ser3627Tyr
|
|
XM_017009964.2:c.10877C>A
|
XP_016865453.1:p.Ser3626Tyr
|
|
XM_017009965.1:c.10877C>A
|
XP_016865454.1:p.Ser3626Tyr
|
|
XM_017009966.2:c.10799C>A
|
XP_016865455.1:p.Ser3600Tyr
|
|
XM_017009967.1:c.10784C>A
|
XP_016865456.1:p.Ser3595Tyr
|
|
XM_017009968.2:c.10880C>A
|
XP_016865457.1:p.Ser3627Tyr
|
|
XM_017009969.2:c.10880C>A
|
XP_016865458.1:p.Ser3627Tyr
|
|
XM_017009970.2:c.10880C>A
|
XP_016865459.1:p.Ser3627Tyr
|
|
XM_017009971.2:c.10880C>A
|
XP_016865460.1:p.Ser3627Tyr
|
|
XM_017009972.1:c.3998C>A
|
XP_016865461.1:p.Ser1333Tyr
|
|
XM_017009973.1:c.3977C>A
|
XP_016865462.1:p.Ser1326Tyr
|
|
XM_017009974.2:c.*81C>A
|
XP_016865463.1:n.*81C>A
|
|
NR_003149.2:n.10875C>A
|
|
|