ENST00000367408.6:n.2905T>G
|
|
|
ENST00000367409.9:c.9618T>G
MANE Select
|
ENSP00000356379.4:p.Ser3206Arg
|
|
ENST00000680265.1:c.9840T>G
|
ENSP00000505384.1:p.Ser3280Arg
|
|
ENST00000680710.1:c.9594T>G
|
ENSP00000506676.1:p.Ser3198Arg
|
|
ENST00000294732.11:c.4863T>G
|
ENSP00000294732.7:p.Ser1621Arg
|
|
ENST00000367408.5:c.2613T>G
|
ENSP00000356378.1:p.Ser871Arg
|
|
ENST00000367409.8:c.9618T>G
|
ENSP00000356379.4:p.Ser3206Arg
|
|
ENST00000612785.1:c.3576T>G
|
ENSP00000479244.1:p.Ser1192Arg
|
|
NM_001206846.1:c.4863T>G
|
NP_001193775.1:p.Ser1621Arg
|
|
NM_018136.4:c.9618T>G
|
NP_060606.3:p.Ser3206Arg
|
|
NM_018136.5:c.9618T>G
MANE Select
|
NP_060606.3:p.Ser3206Arg
|
|
NM_001206846.2:c.4863T>G
|
NP_001193775.1:p.Ser1621Arg
|
|