|
NM_014363.6:c.12538G>T
MANE Select
|
NP_055178.3:p.Glu4180Ter
|
|
ENST00000382292.9:c.12538G>T
MANE Select
|
ENSP00000371729.3:p.Glu4180Ter
|
|
NM_001278055.1:c.12097G>T
|
NP_001264984.1:p.Glu4033Ter
|
|
NM_001278055.2:c.12097G>T
|
NP_001264984.1:p.Glu4033Ter
|
|
NM_014363.5:c.12538G>T
|
NP_055178.3:p.Glu4180Ter
|
|
ENST00000382292.7:c.12538G>T
|
ENSP00000371729.3:p.Glu4180Ter
|
|
ENST00000382298.7:c.12538G>T
|
ENSP00000371735.3:p.Glu4180Ter
|
|
ENST00000402364.1:c.10288G>T
|
ENSP00000385844.1:p.Glu3430Ter
|
|
ENST00000423156.1:c.1058-1854G>T
|
ENSP00000390925.1:n.1058-1854G>T
|
|
ENST00000423156.2:c.2186-1854G>T
|
ENSP00000390925.2:n.2186-1854G>T
|
|
ENST00000455470.5:c.2130-1854G>T
|
|
|
ENST00000455470.6:c.2432-1854G>T
|
ENSP00000406565.2:n.2432-1854G>T
|
|
ENST00000682775.1:c.2186-19223G>T
|
ENSP00000508399.1:n.2186-19223G>T
|
|
ENST00000682944.1:c.12565G>T
|
ENSP00000507173.1:p.Glu4189Ter
|
|
ENST00000683210.1:c.2185+22447G>T
|
ENSP00000506739.1:n.2185+22447G>T
|
|
ENST00000683270.1:c.6446-1854G>T
|
ENSP00000507624.1:n.6446-1854G>T
|
|
ENST00000683367.1:c.2177-1854G>T
|
ENSP00000507780.1:n.2177-1854G>T
|
|
ENST00000683489.1:c.2292-1386G>T
|
ENSP00000508403.1:n.2292-1386G>T
|
|
ENST00000683680.1:c.2319-1386G>T
|
ENSP00000507223.1:n.2319-1386G>T
|
|
ENST00000684163.1:c.2204-1854G>T
|
ENSP00000508262.1:n.2204-1854G>T
|
|
ENST00000684196.1:n.4543-1854G>T
|
|
|
ENST00000684325.1:c.2186-9664G>T
|
ENSP00000508121.1:n.2186-9664G>T
|
|
ENST00000684385.1:c.2221-1854G>T
|
ENSP00000507855.1:n.2221-1854G>T
|
|
ENST00000684497.1:c.2186-8694G>T
|
ENSP00000507057.1:n.2186-8694G>T
|
|
XM_005266338.1:c.12565G>T
|
XP_005266395.1:p.Glu4189Ter
|
|
XM_005266338.2:c.12565G>T
|
XP_005266395.1:p.Glu4189Ter
|
|
XM_011535038.1:c.12589G>T
|
XP_011533340.1:p.Glu4197Ter
|
|
XM_011535039.1:c.12556G>T
|
XP_011533341.1:p.Glu4186Ter
|
|
XM_011535039.2:c.12556G>T
|
XP_011533341.1:p.Glu4186Ter
|
|
XM_017020539.1:c.12529G>T
|
XP_016876028.1:p.Glu4177Ter
|
|
XM_024449337.1:c.12565G>T
|
XP_024305105.1:p.Glu4189Ter
|
