ENST00000645828.1:n.2805G>T
|
|
|
ENST00000651671.1:c.4998G>T
MANE Select
|
ENSP00000498587.1:p.Leu1666=
|
|
ENST00000679595.1:c.4998G>T
|
ENSP00000506241.1:p.Leu1666=
|
|
ENST00000680133.1:c.4884G>T
|
ENSP00000505319.1:p.Leu1628=
|
|
ENST00000680218.1:c.4878G>T
|
ENSP00000505339.1:p.Leu1626=
|
|
ENST00000680668.1:c.4884G>T
|
ENSP00000506336.1:p.Leu1628=
|
|
ENST00000680778.1:c.2595G>T
|
ENSP00000506033.1:p.Leu865=
|
|
ENST00000680924.1:c.*2398G>T
|
ENSP00000506031.1:n.*2398G>T
|
|
ENST00000681135.1:c.*2607G>T
|
ENSP00000506636.1:n.*2607G>T
|
|
ENST00000681298.1:n.1811G>T
|
|
|
ENST00000681454.1:c.*4234G>T
|
ENSP00000505763.1:n.*4234G>T
|
|
ENST00000277541.6:c.4998G>T
|
ENSP00000277541.6:p.Leu1666=
|
|
ENST00000494783.1:n.153G>T
|
|
|
NM_017617.3:c.4998G>T
|
NP_060087.3:p.Leu1666=
|
|
XM_011518717.1:c.4299G>T
|
XP_011517019.1:p.Leu1433=
|
|
NM_017617.5:c.4998G>T
MANE Select
|
NP_060087.3:p.Leu1666=
|
|
XM_011518717.2:c.4275G>T
|
XP_011517019.2:p.Leu1425=
|
|