ENST00000378156.9:c.4024G>T
MANE Select
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ENSP00000367398.4:p.Glu1342Ter
|
|
ENST00000378156.8:c.4024G>T
|
ENSP00000367398.4:p.Glu1342Ter
|
|
ENST00000378161.5:n.3175G>T
|
|
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ENST00000378169.7:c.*2925G>T
|
ENSP00000367411.3:n.*2925G>T
|
|
ENST00000460696.1:n.2772G>T
|
|
|
ENST00000478423.6:n.3756G>T
|
|
|
ENST00000489180.6:c.*1835G>T
|
ENSP00000423747.1:n.*1835G>T
|
|
NM_001291593.1:c.2485G>T
|
NP_001278522.1:p.Glu829Ter
|
|
NM_001291594.1:c.2488G>T
|
NP_001278523.1:p.Glu830Ter
|
|
NM_015102.4:c.4024G>T
|
NP_055917.1:p.Glu1342Ter
|
|
NR_111987.1:n.4839G>T
|
|
|
XM_006710563.2:c.4024G>T
|
XP_006710626.1:p.Glu1342Ter
|
|
XM_006710565.2:c.4024G>T
|
XP_006710628.1:p.Glu1342Ter
|
|
XM_011541213.1:c.4021G>T
|
XP_011539515.1:p.Glu1341Ter
|
|
XM_011541214.1:c.3982G>T
|
XP_011539516.1:p.Glu1328Ter
|
|
XM_011541215.1:c.3913G>T
|
XP_011539517.1:p.Glu1305Ter
|
|
XM_011541216.1:c.4024G>T
|
XP_011539518.1:p.Glu1342Ter
|
|
XM_011541217.1:c.4024G>T
|
XP_011539519.1:p.Glu1342Ter
|
|
XM_011541218.1:c.4024G>T
|
XP_011539520.1:p.Glu1342Ter
|
|
XM_011541219.1:c.3970G>T
|
XP_011539521.1:p.Glu1324Ter
|
|
XM_006710563.3:c.4024G>T
|
XP_006710626.1:p.Glu1342Ter
|
|
XM_011541216.2:c.4024G>T
|
XP_011539518.1:p.Glu1342Ter
|
|
XM_011541217.2:c.4024G>T
|
XP_011539519.1:p.Glu1342Ter
|
|
XM_011541218.2:c.4024G>T
|
XP_011539520.1:p.Glu1342Ter
|
|
XM_017000996.1:c.3979G>T
|
XP_016856485.1:p.Glu1327Ter
|
|
XM_017000997.1:c.4024G>T
|
XP_016856486.1:p.Glu1342Ter
|
|
XM_017000999.1:c.3496G>T
|
XP_016856488.1:p.Glu1166Ter
|
|
XM_017001000.2:c.3496G>T
|
XP_016856489.1:p.Glu1166Ter
|
|
XM_017001001.1:c.3226G>T
|
XP_016856490.1:p.Glu1076Ter
|
|
XM_017001003.1:c.2485G>T
|
XP_016856492.1:p.Glu829Ter
|
|
XR_001737114.1:n.3890G>T
|
|
|
XR_001737115.1:n.3875G>T
|
|
|
NM_015102.5:c.4024G>T
MANE Select
|
NP_055917.1:p.Glu1342Ter
|
|
NM_001291593.2:c.2485G>T
|
NP_001278522.1:p.Glu829Ter
|
|
NM_001291594.2:c.2488G>T
|
NP_001278523.1:p.Glu830Ter
|
|
NR_111987.2:n.4791G>T
|
|
|