ENST00000645828.1:n.2786G>T
|
|
|
ENST00000651671.1:c.4979G>T
MANE Select
|
ENSP00000498587.1:p.Gly1660Val
|
|
ENST00000679595.1:c.4979G>T
|
ENSP00000506241.1:p.Gly1660Val
|
|
ENST00000680133.1:c.4865G>T
|
ENSP00000505319.1:p.Gly1622Val
|
|
ENST00000680218.1:c.4859G>T
|
ENSP00000505339.1:p.Gly1620Val
|
|
ENST00000680668.1:c.4865G>T
|
ENSP00000506336.1:p.Gly1622Val
|
|
ENST00000680778.1:c.2576G>T
|
ENSP00000506033.1:p.Gly859Val
|
|
ENST00000680924.1:c.*2379G>T
|
ENSP00000506031.1:n.*2379G>T
|
|
ENST00000681135.1:c.*2588G>T
|
ENSP00000506636.1:n.*2588G>T
|
|
ENST00000681298.1:n.1792G>T
|
|
|
ENST00000681454.1:c.*4215G>T
|
ENSP00000505763.1:n.*4215G>T
|
|
ENST00000277541.6:c.4979G>T
|
ENSP00000277541.6:p.Gly1660Val
|
|
ENST00000494783.1:n.134G>T
|
|
|
NM_017617.3:c.4979G>T
|
NP_060087.3:p.Gly1660Val
|
|
XM_011518717.1:c.4280G>T
|
XP_011517019.1:p.Gly1427Val
|
|
NM_017617.5:c.4979G>T
MANE Select
|
NP_060087.3:p.Gly1660Val
|
|
XM_011518717.2:c.4256G>T
|
XP_011517019.2:p.Gly1419Val
|
|