ENST00000700484.1:n.2A>G
|
|
|
ENST00000303391.11:c.-119A>G
MANE Plus Clinical
|
ENSP00000301948.6:n.-119A>G
|
|
ENST00000453960.7:c.42A>G
MANE Select
|
ENSP00000395535.2:p.Gly14=
|
|
ENST00000676382.1:n.2A>G
|
|
|
ENST00000303391.10:c.-119A>G
|
ENSP00000301948.6:n.-119A>G
|
|
ENST00000369957.5:c.-119A>G
|
ENSP00000358973.4:n.-119A>G
|
|
ENST00000407218.5:c.42A>G
|
ENSP00000384865.2:p.Gly14=
|
|
ENST00000453960.6:c.42A>G
|
ENSP00000395535.2:p.Gly14=
|
|
ENST00000619732.4:c.-119A>G
|
ENSP00000480973.1:n.-119A>G
|
|
ENST00000627864.1:n.57A>G
|
|
|
ENST00000628176.2:c.-119A>G
|
ENSP00000486978.1:n.-119A>G
|
|
ENST00000631210.1:n.305+7157A>G
|
|
|
NM_001110792.1:c.42A>G
|
NP_001104262.1:p.Gly14=
|
|
NM_001316337.1:c.-566A>G
|
NP_001303266.1:n.-566A>G
|
|
NM_004992.3:c.-119A>G
|
NP_004983.1:n.-119A>G
|
|
XM_005274682.3:c.-510A>G
|
XP_005274739.1:n.-510A>G
|
|
NM_001110792.2:c.42A>G
MANE Select
|
NP_001104262.1:p.Gly14=
|
|
NM_001316337.2:c.-566A>G
|
NP_001303266.1:n.-566A>G
|
|
NM_001369391.2:c.-861A>G
|
NP_001356320.1:n.-861A>G
|
|
NM_001369392.2:c.-510A>G
|
NP_001356321.1:n.-510A>G
|
|
NM_001369393.2:c.-386A>G
|
NP_001356322.1:n.-386A>G
|
|
NM_001386137.1:c.-791A>G
|
NP_001373066.1:n.-791A>G
|
|
NM_001386138.1:c.-679A>G
|
NP_001373067.1:n.-679A>G
|
|
NM_001386139.1:c.-555A>G
|
NP_001373068.1:n.-555A>G
|
|
NM_004992.4:c.-119A>G
MANE Plus Clinical
|
NP_004983.1:n.-119A>G
|
|