ENST00000367408.6:n.3306A=
|
|
|
ENST00000367409.9:c.10019A=
MANE Select
|
ENSP00000356379.4:p.Glu3340=
|
|
ENST00000680265.1:c.10241A=
|
ENSP00000505384.1:p.Glu3414=
|
|
ENST00000680710.1:c.9995A=
|
ENSP00000506676.1:p.Glu3332=
|
|
ENST00000294732.11:c.5264A=
|
ENSP00000294732.7:p.Glu1755=
|
|
ENST00000367408.5:c.3014A=
|
ENSP00000356378.1:p.Glu1005=
|
|
ENST00000367409.8:c.10019A=
|
ENSP00000356379.4:p.Glu3340=
|
|
ENST00000612785.1:c.3977A=
|
ENSP00000479244.1:p.Glu1326=
|
|
NM_001206846.1:c.5264A=
|
NP_001193775.1:p.Glu1755=
|
|
NM_018136.4:c.10019A=
|
NP_060606.3:p.Glu3340=
|
|
NM_018136.5:c.10019A=
MANE Select
|
NP_060606.3:p.Glu3340=
|
|
NM_001206846.2:c.5264A=
|
NP_001193775.1:p.Glu1755=
|
|