ENST00000369975.6:c.3393A>C
|
ENSP00000358992.1:p.Glu1131Asp
|
|
ENST00000369977.8:c.3489A>C
MANE Select
|
ENSP00000358994.3:p.Glu1163Asp
|
|
ENST00000369985.9:c.3420A>C
|
ENSP00000359002.3:p.Glu1140Asp
|
|
ENST00000664640.1:c.3516A>C
|
ENSP00000499278.1:p.Glu1172Asp
|
|
ENST00000671923.1:c.*1500A>C
|
ENSP00000500835.1:n.*1500A>C
|
|
ENST00000672093.1:c.3489A>C
|
ENSP00000500710.1:p.Glu1163Asp
|
|
ENST00000672162.1:n.1655A>C
|
|
|
ENST00000369975.5:c.3393A>C
|
ENSP00000358992.1:p.Glu1131Asp
|
|
ENST00000369977.7:c.3489A>C
|
ENSP00000358994.3:p.Glu1163Asp
|
|
ENST00000369981.7:c.3519A>C
|
ENSP00000358998.4:p.Glu1173Asp
|
|
ENST00000369985.8:c.3420A>C
|
ENSP00000359002.3:p.Glu1140Asp
|
|
ENST00000615563.4:c.3420A>C
|
ENSP00000478013.1:p.Glu1140Asp
|
|
ENST00000627432.2:c.3516A>C
|
ENSP00000487348.1:p.Glu1172Asp
|
|
NM_001300899.1:c.3420A>C
|
NP_001287828.1:p.Glu1140Asp
|
|
NM_004999.3:c.3489A>C
|
NP_004990.3:p.Glu1163Asp
|
|
XM_005248719.2:c.3516A>C
|
XP_005248776.1:p.Glu1172Asp
|
|
XM_005248720.2:c.3489A>C
|
XP_005248777.1:p.Glu1163Asp
|
|
XM_005248721.2:c.3477A>C
|
XP_005248778.1:p.Glu1159Asp
|
|
XM_005248722.2:c.3462A>C
|
XP_005248779.1:p.Glu1154Asp
|
|
XM_005248724.2:c.3450A>C
|
XP_005248781.1:p.Glu1150Asp
|
|
XM_005248726.2:c.3393A>C
|
XP_005248783.1:p.Glu1131Asp
|
|
XM_005248719.4:c.3516A>C
|
XP_005248776.1:p.Glu1172Asp
|
|
XM_005248720.4:c.3489A>C
|
XP_005248777.1:p.Glu1163Asp
|
|
XM_005248721.4:c.3477A>C
|
XP_005248778.1:p.Glu1159Asp
|
|
XM_005248722.4:c.3462A>C
|
XP_005248779.1:p.Glu1154Asp
|
|
XM_005248724.4:c.3450A>C
|
XP_005248781.1:p.Glu1150Asp
|
|
XM_005248726.4:c.3393A>C
|
XP_005248783.1:p.Glu1131Asp
|
|
XM_017010899.2:c.3423A>C
|
XP_016866388.1:p.Glu1141Asp
|
|
XM_024446447.1:c.3516A>C
|
XP_024302215.1:p.Glu1172Asp
|
|
XM_024446448.1:c.3450A>C
|
XP_024302216.1:p.Glu1150Asp
|
|
NM_004999.4:c.3489A>C
MANE Select
|
NP_004990.3:p.Glu1163Asp
|
|
NM_001300899.2:c.3420A>C
|
NP_001287828.1:p.Glu1140Asp
|
|
NM_001368136.1:c.3393A>C
|
NP_001355065.1:p.Glu1131Asp
|
|
NM_001368137.1:c.3450A>C
|
NP_001355066.1:p.Glu1150Asp
|
|
NM_001368138.1:c.3405A>C
|
NP_001355067.1:p.Glu1135Asp
|
|
NM_001368865.1:c.3516A>C
|
NP_001355794.1:p.Glu1172Asp
|
|
NM_001368866.1:c.3489A>C
|
NP_001355795.1:p.Glu1163Asp
|
|
NR_160538.1:n.3718A>C
|
|
|