|
NM_032119.4:c.8778C>A
MANE Select
|
NP_115495.3:p.Tyr2926Ter
|
|
ENST00000405460.9:c.8778C>A
MANE Select
|
ENSP00000384582.2:p.Tyr2926Ter
|
|
NM_032119.3:c.8778C>A
|
NP_115495.3:p.Tyr2926Ter
|
|
NR_003149.1:n.8791C>A
|
|
|
NR_003149.2:n.8794C>A
|
|
|
ENST00000405460.6:c.8778C>A
|
ENSP00000384582.2:p.Tyr2926Ter
|
|
ENST00000509621.1:c.1475C>A
|
|
|
ENST00000639431.1:c.265+32654C>A
|
ENSP00000491057.1:n.265+32654C>A
|
|
ENST00000639473.1:n.4237C>A
|
|
|
ENST00000640012.1:c.2585C>A
|
|
|
ENST00000640374.1:n.1922C>A
|
|
|
ENST00000640403.1:c.6069C>A
|
ENSP00000492531.1:p.Tyr2023Ter
|
|
ENST00000640779.1:c.3507C>A
|
|
|
XM_011543675.1:c.8775C>A
|
XP_011541977.1:p.Tyr2925Ter
|
|
XM_011543676.1:c.8697C>A
|
XP_011541978.1:p.Tyr2899Ter
|
|
XM_011543677.1:c.6081C>A
|
XP_011541979.1:p.Tyr2027Ter
|
|
XM_011543678.1:c.8778C>A
|
XP_011541980.1:p.Tyr2926Ter
|
|
XM_011543679.1:c.8778C>A
|
XP_011541981.1:p.Tyr2926Ter
|
|
XM_017009963.2:c.8799C>A
|
XP_016865452.1:p.Tyr2933Ter
|
|
XM_017009964.2:c.8796C>A
|
XP_016865453.1:p.Tyr2932Ter
|
|
XM_017009965.1:c.8796C>A
|
XP_016865454.1:p.Tyr2932Ter
|
|
XM_017009966.2:c.8718C>A
|
XP_016865455.1:p.Tyr2906Ter
|
|
XM_017009967.1:c.8703C>A
|
XP_016865456.1:p.Tyr2901Ter
|
|
XM_017009968.2:c.8799C>A
|
XP_016865457.1:p.Tyr2933Ter
|
|
XM_017009969.2:c.8799C>A
|
XP_016865458.1:p.Tyr2933Ter
|
|
XM_017009970.2:c.8799C>A
|
XP_016865459.1:p.Tyr2933Ter
|
|
XM_017009971.2:c.8799C>A
|
XP_016865460.1:p.Tyr2933Ter
|
|
XM_017009972.1:c.1917C>A
|
XP_016865461.1:p.Tyr639Ter
|
|
XM_017009973.1:c.1896C>A
|
XP_016865462.1:p.Tyr632Ter
|
|
XM_017009974.2:c.8799C>A
|
XP_016865463.1:p.Tyr2933Ter
|