ENST00000399503.4:c.2781T>A
MANE Select
|
ENSP00000382423.3:p.Ile927=
|
|
ENST00000399503.3:c.2781T>A
|
ENSP00000382423.3:p.Ile927=
|
|
NM_005921.1:c.2781T>A
|
NP_005912.1:p.Ile927=
|
|
XM_005248519.3:c.2403T>A
|
XP_005248576.2:p.Ile801=
|
|
XM_011543406.1:c.2526T>A
|
XP_011541708.1:p.Ile842=
|
|
XM_011543407.1:c.2502T>A
|
XP_011541709.1:p.Ile834=
|
|
XM_011543408.1:c.2781T>A
|
XP_011541710.1:p.Ile927=
|
|
XM_017009484.1:c.2370T>A
|
XP_016864973.1:p.Ile790=
|
|
XM_017009485.1:c.2292T>A
|
XP_016864974.1:p.Ile764=
|
|
XR_001742068.2:n.2812T>A
|
|
|
NM_005921.2:c.2781T>A
MANE Select
|
NP_005912.1:p.Ile927=
|
|