ENST00000367408.6:n.3272T>G
|
|
|
ENST00000367409.9:c.9985T>G
MANE Select
|
ENSP00000356379.4:p.Tyr3329Asp
|
|
ENST00000680265.1:c.10207T>G
|
ENSP00000505384.1:p.Tyr3403Asp
|
|
ENST00000680710.1:c.9961T>G
|
ENSP00000506676.1:p.Tyr3321Asp
|
|
ENST00000294732.11:c.5230T>G
|
ENSP00000294732.7:p.Tyr1744Asp
|
|
ENST00000367408.5:c.2980T>G
|
ENSP00000356378.1:p.Tyr994Asp
|
|
ENST00000367409.8:c.9985T>G
|
ENSP00000356379.4:p.Tyr3329Asp
|
|
ENST00000612785.1:c.3943T>G
|
ENSP00000479244.1:p.Tyr1315Asp
|
|
NM_001206846.1:c.5230T>G
|
NP_001193775.1:p.Tyr1744Asp
|
|
NM_018136.4:c.9985T>G
|
NP_060606.3:p.Tyr3329Asp
|
|
NM_018136.5:c.9985T>G
MANE Select
|
NP_060606.3:p.Tyr3329Asp
|
|
NM_001206846.2:c.5230T>G
|
NP_001193775.1:p.Tyr1744Asp
|
|