ENST00000374479.4:c.1102G>T
MANE Select
|
ENSP00000363603.3:p.Ala368Ser
|
|
ENST00000374479.3:c.1102G>T
|
ENSP00000363603.3:p.Ala368Ser
|
|
NM_000147.4:c.1102G>T
|
NP_000138.2:p.Ala368Ser
|
|
XM_005245821.1:c.727G>T
|
XP_005245878.1:p.Ala243Ser
|
|
XM_011541167.1:c.469G>T
|
XP_011539469.1:p.Ala157Ser
|
|
XM_005245821.3:c.727G>T
|
XP_005245878.1:p.Ala243Ser
|
|
XM_011541167.3:c.469G>T
|
XP_011539469.1:p.Ala157Ser
|
|
XM_017000905.2:c.799G>T
|
XP_016856394.1:p.Ala267Ser
|
|
NM_000147.5:c.1102G>T
MANE Select
|
NP_000138.2:p.Ala368Ser
|
|
NR_174379.1:n.1280G>T
|
|
|
NR_174380.1:n.1329G>T
|
|
|
NR_174381.1:n.1168G>T
|
|
|
NR_174382.1:n.1565G>T
|
|
|