ENST00000367408.6:n.3100G=
|
|
|
ENST00000367409.9:c.9813G=
MANE Select
|
ENSP00000356379.4:p.Glu3271=
|
|
ENST00000680265.1:c.10035G=
|
ENSP00000505384.1:p.Glu3345=
|
|
ENST00000680710.1:c.9789G=
|
ENSP00000506676.1:p.Glu3263=
|
|
ENST00000294732.11:c.5058G=
|
ENSP00000294732.7:p.Glu1686=
|
|
ENST00000367408.5:c.2808G=
|
ENSP00000356378.1:p.Glu936=
|
|
ENST00000367409.8:c.9813G=
|
ENSP00000356379.4:p.Glu3271=
|
|
ENST00000612785.1:c.3771G=
|
ENSP00000479244.1:p.Glu1257=
|
|
NM_001206846.1:c.5058G=
|
NP_001193775.1:p.Glu1686=
|
|
NM_018136.4:c.9813G=
|
NP_060606.3:p.Glu3271=
|
|
NM_018136.5:c.9813G=
MANE Select
|
NP_060606.3:p.Glu3271=
|
|
NM_001206846.2:c.5058G=
|
NP_001193775.1:p.Glu1686=
|
|