|
NM_032119.4:c.3908T>A
MANE Select
|
NP_115495.3:p.Leu1303Ter
|
|
ENST00000405460.9:c.3908T>A
MANE Select
|
ENSP00000384582.2:p.Leu1303Ter
|
|
NM_032119.3:c.3908T>A
|
NP_115495.3:p.Leu1303Ter
|
|
NR_003149.1:n.4004T>A
|
|
|
NR_003149.2:n.4007T>A
|
|
|
ENST00000405460.6:c.3908T>A
|
ENSP00000384582.2:p.Leu1303Ter
|
|
ENST00000504142.1:c.2673T>A
|
|
|
ENST00000504142.2:n.2674T>A
|
|
|
ENST00000639676.1:n.1506T>A
|
|
|
ENST00000640403.1:c.1199T>A
|
ENSP00000492531.1:p.Leu400Ter
|
|
XM_011543675.1:c.3908T>A
|
XP_011541977.1:p.Leu1303Ter
|
|
XM_011543676.1:c.3908T>A
|
XP_011541978.1:p.Leu1303Ter
|
|
XM_011543677.1:c.1211T>A
|
XP_011541979.1:p.Leu404Ter
|
|
XM_011543678.1:c.3908T>A
|
XP_011541980.1:p.Leu1303Ter
|
|
XM_011543679.1:c.3908T>A
|
XP_011541981.1:p.Leu1303Ter
|
|
XM_017009963.2:c.3908T>A
|
XP_016865452.1:p.Leu1303Ter
|
|
XM_017009964.2:c.3908T>A
|
XP_016865453.1:p.Leu1303Ter
|
|
XM_017009965.1:c.3905T>A
|
XP_016865454.1:p.Leu1302Ter
|
|
XM_017009966.2:c.3908T>A
|
XP_016865455.1:p.Leu1303Ter
|
|
XM_017009967.1:c.3812T>A
|
XP_016865456.1:p.Leu1271Ter
|
|
XM_017009968.2:c.3908T>A
|
XP_016865457.1:p.Leu1303Ter
|
|
XM_017009969.2:c.3908T>A
|
XP_016865458.1:p.Leu1303Ter
|
|
XM_017009970.2:c.3908T>A
|
XP_016865459.1:p.Leu1303Ter
|
|
XM_017009971.2:c.3908T>A
|
XP_016865460.1:p.Leu1303Ter
|
|
XM_017009974.2:c.3908T>A
|
XP_016865463.1:p.Leu1303Ter
|