ENST00000367408.6:n.2486G=
|
|
|
ENST00000367409.9:c.9199G=
MANE Select
|
ENSP00000356379.4:p.Glu3067=
|
|
ENST00000680265.1:c.9421G=
|
ENSP00000505384.1:p.Glu3141=
|
|
ENST00000680710.1:c.9199G=
|
ENSP00000506676.1:p.Glu3067=
|
|
ENST00000294732.11:c.4444G=
|
ENSP00000294732.7:p.Glu1482=
|
|
ENST00000367408.5:c.2194G=
|
ENSP00000356378.1:p.Glu732=
|
|
ENST00000367409.8:c.9199G=
|
ENSP00000356379.4:p.Glu3067=
|
|
ENST00000612785.1:c.3157G=
|
ENSP00000479244.1:p.Glu1053=
|
|
NM_001206846.1:c.4444G=
|
NP_001193775.1:p.Glu1482=
|
|
NM_018136.4:c.9199G=
|
NP_060606.3:p.Glu3067=
|
|
NM_018136.5:c.9199G=
MANE Select
|
NP_060606.3:p.Glu3067=
|
|
NM_001206846.2:c.4444G=
|
NP_001193775.1:p.Glu1482=
|
|