|
NM_032119.4:c.3941T>A
MANE Select
|
NP_115495.3:p.Leu1314Ter
|
|
ENST00000405460.9:c.3941T>A
MANE Select
|
ENSP00000384582.2:p.Leu1314Ter
|
|
NM_032119.3:c.3941T>A
|
NP_115495.3:p.Leu1314Ter
|
|
NR_003149.1:n.4037T>A
|
|
|
NR_003149.2:n.4040T>A
|
|
|
ENST00000405460.6:c.3941T>A
|
ENSP00000384582.2:p.Leu1314Ter
|
|
ENST00000504142.1:c.2706T>A
|
|
|
ENST00000504142.2:n.2707T>A
|
|
|
ENST00000639676.1:n.1539T>A
|
|
|
ENST00000640403.1:c.1232T>A
|
ENSP00000492531.1:p.Leu411Ter
|
|
XM_011543675.1:c.3941T>A
|
XP_011541977.1:p.Leu1314Ter
|
|
XM_011543676.1:c.3941T>A
|
XP_011541978.1:p.Leu1314Ter
|
|
XM_011543677.1:c.1244T>A
|
XP_011541979.1:p.Leu415Ter
|
|
XM_011543678.1:c.3941T>A
|
XP_011541980.1:p.Leu1314Ter
|
|
XM_011543679.1:c.3941T>A
|
XP_011541981.1:p.Leu1314Ter
|
|
XM_017009963.2:c.3941T>A
|
XP_016865452.1:p.Leu1314Ter
|
|
XM_017009964.2:c.3941T>A
|
XP_016865453.1:p.Leu1314Ter
|
|
XM_017009965.1:c.3938T>A
|
XP_016865454.1:p.Leu1313Ter
|
|
XM_017009966.2:c.3941T>A
|
XP_016865455.1:p.Leu1314Ter
|
|
XM_017009967.1:c.3845T>A
|
XP_016865456.1:p.Leu1282Ter
|
|
XM_017009968.2:c.3941T>A
|
XP_016865457.1:p.Leu1314Ter
|
|
XM_017009969.2:c.3941T>A
|
XP_016865458.1:p.Leu1314Ter
|
|
XM_017009970.2:c.3941T>A
|
XP_016865459.1:p.Leu1314Ter
|
|
XM_017009971.2:c.3941T>A
|
XP_016865460.1:p.Leu1314Ter
|
|
XM_017009974.2:c.3941T>A
|
XP_016865463.1:p.Leu1314Ter
|