ENST00000399503.4:c.2997A>T
MANE Select
|
ENSP00000382423.3:p.Thr999=
|
|
ENST00000399503.3:c.2997A>T
|
ENSP00000382423.3:p.Thr999=
|
|
NM_005921.1:c.2997A>T
|
NP_005912.1:p.Thr999=
|
|
XM_005248519.3:c.2619A>T
|
XP_005248576.2:p.Thr873=
|
|
XM_011543406.1:c.2742A>T
|
XP_011541708.1:p.Thr914=
|
|
XM_011543407.1:c.2718A>T
|
XP_011541709.1:p.Thr906=
|
|
XM_011543408.1:c.2997A>T
|
XP_011541710.1:p.Thr999=
|
|
XM_017009484.1:c.2586A>T
|
XP_016864973.1:p.Thr862=
|
|
XM_017009485.1:c.2508A>T
|
XP_016864974.1:p.Thr836=
|
|
XR_001742068.2:n.3028A>T
|
|
|
NM_005921.2:c.2997A>T
MANE Select
|
NP_005912.1:p.Thr999=
|
|