ENST00000367408.6:n.3313T>G
|
|
|
ENST00000367409.9:c.10026T>G
MANE Select
|
ENSP00000356379.4:p.Cys3342Trp
|
|
ENST00000680265.1:c.10248T>G
|
ENSP00000505384.1:p.Cys3416Trp
|
|
ENST00000680710.1:c.10002T>G
|
ENSP00000506676.1:p.Cys3334Trp
|
|
ENST00000294732.11:c.5271T>G
|
ENSP00000294732.7:p.Cys1757Trp
|
|
ENST00000367408.5:c.3021T>G
|
ENSP00000356378.1:p.Cys1007Trp
|
|
ENST00000367409.8:c.10026T>G
|
ENSP00000356379.4:p.Cys3342Trp
|
|
ENST00000612785.1:c.3984T>G
|
ENSP00000479244.1:p.Cys1328Trp
|
|
NM_001206846.1:c.5271T>G
|
NP_001193775.1:p.Cys1757Trp
|
|
NM_018136.4:c.10026T>G
|
NP_060606.3:p.Cys3342Trp
|
|
NM_018136.5:c.10026T>G
MANE Select
|
NP_060606.3:p.Cys3342Trp
|
|
NM_001206846.2:c.5271T>G
|
NP_001193775.1:p.Cys1757Trp
|
|