ENST00000622443.3:c.840G>C
|
ENSP00000482268.2:p.Thr280=
|
|
ENST00000532059.6:c.843G>C
MANE Select
|
ENSP00000435712.1:p.Thr281=
|
|
ENST00000335135.8:c.840G>C
|
ENSP00000334458.4:p.Thr280=
|
|
ENST00000526716.5:c.222G>C
|
ENSP00000435347.1:p.Thr74=
|
|
ENST00000528712.5:c.222G>C
|
ENSP00000435043.1:p.Thr74=
|
|
ENST00000532059.5:c.843G>C
|
ENSP00000435712.1:p.Thr281=
|
|
ENST00000622443.2:c.837G>C
|
ENSP00000482268.1:p.Thr279=
|
|
NM_001308093.1:c.843G>C
|
NP_001295022.1:p.Thr281=
|
|
NM_001308094.1:c.222G>C
|
NP_001295023.1:p.Thr74=
|
|
NM_002052.3:c.840G>C
|
NP_002043.2:p.Thr280=
|
|
NM_002052.4:c.840G>C
|
NP_002043.2:p.Thr280=
|
|
XM_005272385.3:c.843G>C
|
XP_005272442.1:p.Thr281=
|
|
XM_005272386.1:c.843G>C
|
XP_005272443.1:p.Thr281=
|
|
XM_006716248.1:c.843G>C
|
XP_006716311.1:p.Thr281=
|
|
XM_011543817.1:c.843G>C
|
XP_011542119.1:p.Thr281=
|
|
XM_011543818.1:c.843G>C
|
XP_011542120.1:p.Thr281=
|
|
XM_005272385.4:c.843G>C
|
XP_005272442.1:p.Thr281=
|
|
XM_011543817.3:c.843G>C
|
XP_011542119.1:p.Thr281=
|
|
XM_011543818.2:c.843G>C
|
XP_011542120.1:p.Thr281=
|
|
XM_017013312.2:c.843G>C
|
XP_016868801.1:p.Thr281=
|
|
NM_001308093.3:c.843G>C
MANE Select
|
NP_001295022.1:p.Thr281=
|
|
NM_001308094.2:c.222G>C
|
NP_001295023.1:p.Thr74=
|
|
NM_001374273.1:c.222G>C
|
NP_001361202.1:p.Thr74=
|
|
NM_001374274.1:c.165+1082G>C
|
NP_001361203.1:n.165+1082G>C
|
|
NM_002052.5:c.840G>C
|
NP_002043.2:p.Thr280=
|
|