ENST00000399503.4:c.2560C>T
MANE Select
|
ENSP00000382423.3:p.Arg854Cys
|
|
ENST00000399503.3:c.2560C>T
|
ENSP00000382423.3:p.Arg854Cys
|
|
NM_005921.1:c.2560C>T
|
NP_005912.1:p.Arg854Cys
|
|
XM_005248519.3:c.2182C>T
|
XP_005248576.2:p.Arg728Cys
|
|
XM_011543406.1:c.2305C>T
|
XP_011541708.1:p.Arg769Cys
|
|
XM_011543407.1:c.2281C>T
|
XP_011541709.1:p.Arg761Cys
|
|
XM_011543408.1:c.2560C>T
|
XP_011541710.1:p.Arg854Cys
|
|
XM_017009484.1:c.2149C>T
|
XP_016864973.1:p.Arg717Cys
|
|
XM_017009485.1:c.2071C>T
|
XP_016864974.1:p.Arg691Cys
|
|
XR_001742068.2:n.2591C>T
|
|
|
NM_005921.2:c.2560C>T
MANE Select
|
NP_005912.1:p.Arg854Cys
|
|