ENST00000399503.4:c.819A>T
MANE Select
|
ENSP00000382423.3:p.Arg273Ser
|
|
ENST00000399503.3:c.819A>T
|
ENSP00000382423.3:p.Arg273Ser
|
|
NM_005921.1:c.819A>T
|
NP_005912.1:p.Arg273Ser
|
|
XM_005248519.3:c.441A>T
|
XP_005248576.2:p.Arg147Ser
|
|
XM_011543406.1:c.564A>T
|
XP_011541708.1:p.Arg188Ser
|
|
XM_011543407.1:c.819A>T
|
XP_011541709.1:p.Arg273Ser
|
|
XM_011543408.1:c.819A>T
|
XP_011541710.1:p.Arg273Ser
|
|
XM_017009484.1:c.408A>T
|
XP_016864973.1:p.Arg136Ser
|
|
XM_017009485.1:c.330A>T
|
XP_016864974.1:p.Arg110Ser
|
|
XR_001742068.2:n.850A>T
|
|
|
NM_005921.2:c.819A>T
MANE Select
|
NP_005912.1:p.Arg273Ser
|
|