ENST00000372808.4:c.201C>A
MANE Select
|
ENSP00000361894.3:p.Gly67=
|
|
ENST00000372808.3:c.201C>A
|
ENSP00000361894.3:p.Gly67=
|
|
NM_018960.4:c.201C>A
|
NP_061833.1:p.Gly67=
|
|
XM_011514493.1:c.-13-1244C>A
|
XP_011512795.1:n.-13-1244C>A
|
|
XM_011514494.1:c.-13-1244C>A
|
XP_011512796.1:n.-13-1244C>A
|
|
NM_001318856.1:c.9-1244C>A
|
NP_001305785.1:n.9-1244C>A
|
|
NM_001318857.1:c.152-1794C>A
|
NP_001305786.1:n.152-1794C>A
|
|
NM_001318858.1:c.152-1794C>A
|
NP_001305787.1:n.152-1794C>A
|
|
NM_001318865.1:c.201C>A
|
NP_001305794.1:p.Gly67=
|
|
NM_018960.5:c.201C>A
|
NP_061833.1:p.Gly67=
|
|
NR_134890.1:n.690-1794C>A
|
|
|
NR_134891.1:n.593-1794C>A
|
|
|
NR_134892.1:n.593-1244C>A
|
|
|
NR_134899.1:n.215C>A
|
|
|
NM_018960.6:c.201C>A
MANE Select
|
NP_061833.1:p.Gly67=
|
|
NM_001318856.2:c.9-1244C>A
|
NP_001305785.1:n.9-1244C>A
|
|
NM_001318857.2:c.152-1794C>A
|
NP_001305786.1:n.152-1794C>A
|
|
NM_001318858.2:c.152-1794C>A
|
NP_001305787.1:n.152-1794C>A
|
|
NM_001318865.2:c.201C>A
|
NP_001305794.1:p.Gly67=
|
|
NR_134890.2:n.340-1794C>A
|
|
|
NR_134891.2:n.243-1794C>A
|
|
|
NR_134892.2:n.243-1244C>A
|
|
|
NR_134899.2:n.215C>A
|
|
|