ENST00000645828.1:n.2466G>C
|
|
|
ENST00000651671.1:c.4659G>C
MANE Select
|
ENSP00000498587.1:p.Glu1553Asp
|
|
ENST00000679595.1:c.4659G>C
|
ENSP00000506241.1:p.Glu1553Asp
|
|
ENST00000680133.1:c.4545G>C
|
ENSP00000505319.1:p.Glu1515Asp
|
|
ENST00000680218.1:c.4539G>C
|
ENSP00000505339.1:p.Glu1513Asp
|
|
ENST00000680668.1:c.4545G>C
|
ENSP00000506336.1:p.Glu1515Asp
|
|
ENST00000680778.1:c.2256G>C
|
ENSP00000506033.1:p.Glu752Asp
|
|
ENST00000680924.1:c.*2059G>C
|
ENSP00000506031.1:n.*2059G>C
|
|
ENST00000681135.1:c.*2268G>C
|
ENSP00000506636.1:n.*2268G>C
|
|
ENST00000681298.1:n.1472G>C
|
|
|
ENST00000681454.1:c.*3895G>C
|
ENSP00000505763.1:n.*3895G>C
|
|
ENST00000277541.6:c.4659G>C
|
ENSP00000277541.6:p.Glu1553Asp
|
|
NM_017617.3:c.4659G>C
|
NP_060087.3:p.Glu1553Asp
|
|
XM_011518717.1:c.3960G>C
|
XP_011517019.1:p.Glu1320Asp
|
|
NM_017617.5:c.4659G>C
MANE Select
|
NP_060087.3:p.Glu1553Asp
|
|
XM_011518717.2:c.3936G>C
|
XP_011517019.2:p.Glu1312Asp
|
|