ENST00000405460.9:c.9425T>A
MANE Select
|
ENSP00000384582.2:p.Leu3142Ter
|
|
ENST00000639431.1:c.265+40498T>A
|
ENSP00000491057.1:n.265+40498T>A
|
|
ENST00000639473.1:n.4884T>A
|
|
|
ENST00000640012.1:c.3232T>A
|
|
|
ENST00000640374.1:n.2569T>A
|
|
|
ENST00000640779.1:c.4154T>A
|
|
|
ENST00000405460.6:c.9425T>A
|
ENSP00000384582.2:p.Leu3142Ter
|
|
ENST00000509621.1:c.2122T>A
|
|
|
NM_032119.3:c.9425T>A
|
NP_115495.3:p.Leu3142Ter
|
|
NR_003149.1:n.9438T>A
|
|
|
XM_011543675.1:c.9422T>A
|
XP_011541977.1:p.Leu3141Ter
|
|
XM_011543676.1:c.9344T>A
|
XP_011541978.1:p.Leu3115Ter
|
|
XM_011543677.1:c.6728T>A
|
XP_011541979.1:p.Leu2243Ter
|
|
XM_011543678.1:c.9425T>A
|
XP_011541980.1:p.Leu3142Ter
|
|
XM_011543679.1:c.9425T>A
|
XP_011541981.1:p.Leu3142Ter
|
|
XR_948560.1:n.272-898A>T
|
|
|
NM_032119.4:c.9425T>A
MANE Select
|
NP_115495.3:p.Leu3142Ter
|
|
XM_017009963.2:c.9446T>A
|
XP_016865452.1:p.Leu3149Ter
|
|
XM_017009964.2:c.9443T>A
|
XP_016865453.1:p.Leu3148Ter
|
|
XM_017009965.1:c.9443T>A
|
XP_016865454.1:p.Leu3148Ter
|
|
XM_017009966.2:c.9365T>A
|
XP_016865455.1:p.Leu3122Ter
|
|
XM_017009967.1:c.9350T>A
|
XP_016865456.1:p.Leu3117Ter
|
|
XM_017009968.2:c.9446T>A
|
XP_016865457.1:p.Leu3149Ter
|
|
XM_017009969.2:c.9446T>A
|
XP_016865458.1:p.Leu3149Ter
|
|
XM_017009970.2:c.9446T>A
|
XP_016865459.1:p.Leu3149Ter
|
|
XM_017009971.2:c.9446T>A
|
XP_016865460.1:p.Leu3149Ter
|
|
XM_017009972.1:c.2564T>A
|
XP_016865461.1:p.Leu855Ter
|
|
XM_017009973.1:c.2543T>A
|
XP_016865462.1:p.Leu848Ter
|
|
XM_017009974.2:c.9446T>A
|
XP_016865463.1:p.Leu3149Ter
|
|
XR_001742802.1:n.2523-898A>T
|
|
|
NR_003149.2:n.9441T>A
|
|
|