ENST00000399503.4:c.2560C>A
MANE Select
|
ENSP00000382423.3:p.Arg854Ser
|
|
ENST00000399503.3:c.2560C>A
|
ENSP00000382423.3:p.Arg854Ser
|
|
NM_005921.1:c.2560C>A
|
NP_005912.1:p.Arg854Ser
|
|
XM_005248519.3:c.2182C>A
|
XP_005248576.2:p.Arg728Ser
|
|
XM_011543406.1:c.2305C>A
|
XP_011541708.1:p.Arg769Ser
|
|
XM_011543407.1:c.2281C>A
|
XP_011541709.1:p.Arg761Ser
|
|
XM_011543408.1:c.2560C>A
|
XP_011541710.1:p.Arg854Ser
|
|
XM_017009484.1:c.2149C>A
|
XP_016864973.1:p.Arg717Ser
|
|
XM_017009485.1:c.2071C>A
|
XP_016864974.1:p.Arg691Ser
|
|
XR_001742068.2:n.2591C>A
|
|
|
NM_005921.2:c.2560C>A
MANE Select
|
NP_005912.1:p.Arg854Ser
|
|