ENST00000645828.1:n.2801A>T
|
|
|
ENST00000651671.1:c.4994A>T
MANE Select
|
ENSP00000498587.1:p.Glu1665Val
|
|
ENST00000679595.1:c.4994A>T
|
ENSP00000506241.1:p.Glu1665Val
|
|
ENST00000680133.1:c.4880A>T
|
ENSP00000505319.1:p.Glu1627Val
|
|
ENST00000680218.1:c.4874A>T
|
ENSP00000505339.1:p.Glu1625Val
|
|
ENST00000680668.1:c.4880A>T
|
ENSP00000506336.1:p.Glu1627Val
|
|
ENST00000680778.1:c.2591A>T
|
ENSP00000506033.1:p.Glu864Val
|
|
ENST00000680924.1:c.*2394A>T
|
ENSP00000506031.1:n.*2394A>T
|
|
ENST00000681135.1:c.*2603A>T
|
ENSP00000506636.1:n.*2603A>T
|
|
ENST00000681298.1:n.1807A>T
|
|
|
ENST00000681454.1:c.*4230A>T
|
ENSP00000505763.1:n.*4230A>T
|
|
ENST00000277541.6:c.4994A>T
|
ENSP00000277541.6:p.Glu1665Val
|
|
ENST00000494783.1:n.149A>T
|
|
|
NM_017617.3:c.4994A>T
|
NP_060087.3:p.Glu1665Val
|
|
XM_011518717.1:c.4295A>T
|
XP_011517019.1:p.Glu1432Val
|
|
NM_017617.5:c.4994A>T
MANE Select
|
NP_060087.3:p.Glu1665Val
|
|
XM_011518717.2:c.4271A>T
|
XP_011517019.2:p.Glu1424Val
|
|