ENST00000405460.9:c.9385G>T
MANE Select
|
ENSP00000384582.2:p.Glu3129Ter
|
|
ENST00000639431.1:c.265+40458G>T
|
ENSP00000491057.1:n.265+40458G>T
|
|
ENST00000639473.1:n.4844G>T
|
|
|
ENST00000640012.1:c.3192G>T
|
|
|
ENST00000640374.1:n.2529G>T
|
|
|
ENST00000640779.1:c.4114G>T
|
|
|
ENST00000405460.6:c.9385G>T
|
ENSP00000384582.2:p.Glu3129Ter
|
|
ENST00000509621.1:c.2082G>T
|
|
|
NM_032119.3:c.9385G>T
|
NP_115495.3:p.Glu3129Ter
|
|
NR_003149.1:n.9398G>T
|
|
|
XM_011543675.1:c.9382G>T
|
XP_011541977.1:p.Glu3128Ter
|
|
XM_011543676.1:c.9304G>T
|
XP_011541978.1:p.Glu3102Ter
|
|
XM_011543677.1:c.6688G>T
|
XP_011541979.1:p.Glu2230Ter
|
|
XM_011543678.1:c.9385G>T
|
XP_011541980.1:p.Glu3129Ter
|
|
XM_011543679.1:c.9385G>T
|
XP_011541981.1:p.Glu3129Ter
|
|
XR_948560.1:n.272-858C>A
|
|
|
NM_032119.4:c.9385G>T
MANE Select
|
NP_115495.3:p.Glu3129Ter
|
|
XM_017009963.2:c.9406G>T
|
XP_016865452.1:p.Glu3136Ter
|
|
XM_017009964.2:c.9403G>T
|
XP_016865453.1:p.Glu3135Ter
|
|
XM_017009965.1:c.9403G>T
|
XP_016865454.1:p.Glu3135Ter
|
|
XM_017009966.2:c.9325G>T
|
XP_016865455.1:p.Glu3109Ter
|
|
XM_017009967.1:c.9310G>T
|
XP_016865456.1:p.Glu3104Ter
|
|
XM_017009968.2:c.9406G>T
|
XP_016865457.1:p.Glu3136Ter
|
|
XM_017009969.2:c.9406G>T
|
XP_016865458.1:p.Glu3136Ter
|
|
XM_017009970.2:c.9406G>T
|
XP_016865459.1:p.Glu3136Ter
|
|
XM_017009971.2:c.9406G>T
|
XP_016865460.1:p.Glu3136Ter
|
|
XM_017009972.1:c.2524G>T
|
XP_016865461.1:p.Glu842Ter
|
|
XM_017009973.1:c.2503G>T
|
XP_016865462.1:p.Glu835Ter
|
|
XM_017009974.2:c.9406G>T
|
XP_016865463.1:p.Glu3136Ter
|
|
XR_001742802.1:n.2523-858C>A
|
|
|
NR_003149.2:n.9401G>T
|
|
|