ENST00000367408.6:n.3311T>G
|
|
|
ENST00000367409.9:c.10024T>G
MANE Select
|
ENSP00000356379.4:p.Cys3342Gly
|
|
ENST00000680265.1:c.10246T>G
|
ENSP00000505384.1:p.Cys3416Gly
|
|
ENST00000680710.1:c.10000T>G
|
ENSP00000506676.1:p.Cys3334Gly
|
|
ENST00000294732.11:c.5269T>G
|
ENSP00000294732.7:p.Cys1757Gly
|
|
ENST00000367408.5:c.3019T>G
|
ENSP00000356378.1:p.Cys1007Gly
|
|
ENST00000367409.8:c.10024T>G
|
ENSP00000356379.4:p.Cys3342Gly
|
|
ENST00000612785.1:c.3982T>G
|
ENSP00000479244.1:p.Cys1328Gly
|
|
NM_001206846.1:c.5269T>G
|
NP_001193775.1:p.Cys1757Gly
|
|
NM_018136.4:c.10024T>G
|
NP_060606.3:p.Cys3342Gly
|
|
NM_018136.5:c.10024T>G
MANE Select
|
NP_060606.3:p.Cys3342Gly
|
|
NM_001206846.2:c.5269T>G
|
NP_001193775.1:p.Cys1757Gly
|
|