ENST00000327892.13:c.792T>C
MANE Select
|
ENSP00000339001.7:p.His264=
|
|
ENST00000680530.1:n.1654T>C
|
|
|
ENST00000681421.1:n.1858T>C
|
|
|
ENST00000681435.1:c.576T>C
|
ENSP00000506665.1:p.His192=
|
|
ENST00000327892.12:c.792T>C
|
ENSP00000339001.7:p.His264=
|
|
ENST00000330914.7:c.576T>C
|
ENSP00000365578.2:p.His192=
|
|
ENST00000396384.1:c.576T>C
|
ENSP00000379668.1:p.His192=
|
|
ENST00000396389.5:c.738T>C
|
ENSP00000379672.1:p.His246=
|
|
NM_001293212.1:c.852T>C
|
NP_001280141.1:p.His284=
|
|
NM_001293213.1:c.370-184T>C
|
NP_001280142.1:n.370-184T>C
|
|
NM_001293214.1:c.660T>C
|
NP_001280143.1:p.His220=
|
|
NM_001293215.1:c.576T>C
|
NP_001280144.1:p.His192=
|
|
NM_001293216.1:c.576T>C
|
NP_001280145.1:p.His192=
|
|
NM_178014.3:c.792T>C
|
NP_821133.1:p.His264=
|
|
NR_120608.1:n.584-85T>C
|
|
|
NM_178014.4:c.792T>C
MANE Select
|
NP_821133.1:p.His264=
|
|
NM_001293212.2:c.852T>C
|
NP_001280141.1:p.His284=
|
|
NM_001293213.2:c.370-184T>C
|
NP_001280142.1:n.370-184T>C
|
|
NM_001293214.2:c.660T>C
|
NP_001280143.1:p.His220=
|
|
NM_001293215.2:c.576T>C
|
NP_001280144.1:p.His192=
|
|
NM_001293216.2:c.576T>C
|
NP_001280145.1:p.His192=
|
|
NR_120608.2:n.433-85T>C
|
|
|