ENST00000645828.1:n.2781G>C
|
|
|
ENST00000651671.1:c.4974G>C
MANE Select
|
ENSP00000498587.1:p.Glu1658Asp
|
|
ENST00000679595.1:c.4974G>C
|
ENSP00000506241.1:p.Glu1658Asp
|
|
ENST00000680133.1:c.4860G>C
|
ENSP00000505319.1:p.Glu1620Asp
|
|
ENST00000680218.1:c.4854G>C
|
ENSP00000505339.1:p.Glu1618Asp
|
|
ENST00000680668.1:c.4860G>C
|
ENSP00000506336.1:p.Glu1620Asp
|
|
ENST00000680778.1:c.2571G>C
|
ENSP00000506033.1:p.Glu857Asp
|
|
ENST00000680924.1:c.*2374G>C
|
ENSP00000506031.1:n.*2374G>C
|
|
ENST00000681135.1:c.*2583G>C
|
ENSP00000506636.1:n.*2583G>C
|
|
ENST00000681298.1:n.1787G>C
|
|
|
ENST00000681454.1:c.*4210G>C
|
ENSP00000505763.1:n.*4210G>C
|
|
ENST00000277541.6:c.4974G>C
|
ENSP00000277541.6:p.Glu1658Asp
|
|
ENST00000494783.1:n.129G>C
|
|
|
NM_017617.3:c.4974G>C
|
NP_060087.3:p.Glu1658Asp
|
|
XM_011518717.1:c.4275G>C
|
XP_011517019.1:p.Glu1425Asp
|
|
NM_017617.5:c.4974G>C
MANE Select
|
NP_060087.3:p.Glu1658Asp
|
|
XM_011518717.2:c.4251G>C
|
XP_011517019.2:p.Glu1417Asp
|
|