ENST00000378156.9:c.4024G>C
MANE Select
|
ENSP00000367398.4:p.Glu1342Gln
|
|
ENST00000378156.8:c.4024G>C
|
ENSP00000367398.4:p.Glu1342Gln
|
|
ENST00000378161.5:n.3175G>C
|
|
|
ENST00000378169.7:c.*2925G>C
|
ENSP00000367411.3:n.*2925G>C
|
|
ENST00000460696.1:n.2772G>C
|
|
|
ENST00000478423.6:n.3756G>C
|
|
|
ENST00000489180.6:c.*1835G>C
|
ENSP00000423747.1:n.*1835G>C
|
|
NM_001291593.1:c.2485G>C
|
NP_001278522.1:p.Glu829Gln
|
|
NM_001291594.1:c.2488G>C
|
NP_001278523.1:p.Glu830Gln
|
|
NM_015102.4:c.4024G>C
|
NP_055917.1:p.Glu1342Gln
|
|
NR_111987.1:n.4839G>C
|
|
|
XM_006710563.2:c.4024G>C
|
XP_006710626.1:p.Glu1342Gln
|
|
XM_006710565.2:c.4024G>C
|
XP_006710628.1:p.Glu1342Gln
|
|
XM_011541213.1:c.4021G>C
|
XP_011539515.1:p.Glu1341Gln
|
|
XM_011541214.1:c.3982G>C
|
XP_011539516.1:p.Glu1328Gln
|
|
XM_011541215.1:c.3913G>C
|
XP_011539517.1:p.Glu1305Gln
|
|
XM_011541216.1:c.4024G>C
|
XP_011539518.1:p.Glu1342Gln
|
|
XM_011541217.1:c.4024G>C
|
XP_011539519.1:p.Glu1342Gln
|
|
XM_011541218.1:c.4024G>C
|
XP_011539520.1:p.Glu1342Gln
|
|
XM_011541219.1:c.3970G>C
|
XP_011539521.1:p.Glu1324Gln
|
|
XM_006710563.3:c.4024G>C
|
XP_006710626.1:p.Glu1342Gln
|
|
XM_011541216.2:c.4024G>C
|
XP_011539518.1:p.Glu1342Gln
|
|
XM_011541217.2:c.4024G>C
|
XP_011539519.1:p.Glu1342Gln
|
|
XM_011541218.2:c.4024G>C
|
XP_011539520.1:p.Glu1342Gln
|
|
XM_017000996.1:c.3979G>C
|
XP_016856485.1:p.Glu1327Gln
|
|
XM_017000997.1:c.4024G>C
|
XP_016856486.1:p.Glu1342Gln
|
|
XM_017000999.1:c.3496G>C
|
XP_016856488.1:p.Glu1166Gln
|
|
XM_017001000.2:c.3496G>C
|
XP_016856489.1:p.Glu1166Gln
|
|
XM_017001001.1:c.3226G>C
|
XP_016856490.1:p.Glu1076Gln
|
|
XM_017001003.1:c.2485G>C
|
XP_016856492.1:p.Glu829Gln
|
|
XR_001737114.1:n.3890G>C
|
|
|
XR_001737115.1:n.3875G>C
|
|
|
NM_015102.5:c.4024G>C
MANE Select
|
NP_055917.1:p.Glu1342Gln
|
|
NM_001291593.2:c.2485G>C
|
NP_001278522.1:p.Glu829Gln
|
|
NM_001291594.2:c.2488G>C
|
NP_001278523.1:p.Glu830Gln
|
|
NR_111987.2:n.4791G>C
|
|
|