ENST00000700484.1:n.5A>T
|
|
|
ENST00000303391.11:c.-116A>T
MANE Plus Clinical
|
ENSP00000301948.6:n.-116A>T
|
|
ENST00000453960.7:c.45A>T
MANE Select
|
ENSP00000395535.2:p.Gly15=
|
|
ENST00000676382.1:n.5A>T
|
|
|
ENST00000303391.10:c.-116A>T
|
ENSP00000301948.6:n.-116A>T
|
|
ENST00000369957.5:c.-116A>T
|
ENSP00000358973.4:n.-116A>T
|
|
ENST00000407218.5:c.45A>T
|
ENSP00000384865.2:p.Gly15=
|
|
ENST00000453960.6:c.45A>T
|
ENSP00000395535.2:p.Gly15=
|
|
ENST00000619732.4:c.-116A>T
|
ENSP00000480973.1:n.-116A>T
|
|
ENST00000627864.1:n.60A>T
|
|
|
ENST00000628176.2:c.-116A>T
|
ENSP00000486978.1:n.-116A>T
|
|
ENST00000631210.1:n.305+7160A>T
|
|
|
NM_001110792.1:c.45A>T
|
NP_001104262.1:p.Gly15=
|
|
NM_001316337.1:c.-563A>T
|
NP_001303266.1:n.-563A>T
|
|
NM_004992.3:c.-116A>T
|
NP_004983.1:n.-116A>T
|
|
XM_005274682.3:c.-507A>T
|
XP_005274739.1:n.-507A>T
|
|
NM_001110792.2:c.45A>T
MANE Select
|
NP_001104262.1:p.Gly15=
|
|
NM_001316337.2:c.-563A>T
|
NP_001303266.1:n.-563A>T
|
|
NM_001369391.2:c.-858A>T
|
NP_001356320.1:n.-858A>T
|
|
NM_001369392.2:c.-507A>T
|
NP_001356321.1:n.-507A>T
|
|
NM_001369393.2:c.-383A>T
|
NP_001356322.1:n.-383A>T
|
|
NM_001386137.1:c.-788A>T
|
NP_001373066.1:n.-788A>T
|
|
NM_001386138.1:c.-676A>T
|
NP_001373067.1:n.-676A>T
|
|
NM_001386139.1:c.-552A>T
|
NP_001373068.1:n.-552A>T
|
|
NM_004992.4:c.-116A>T
MANE Plus Clinical
|
NP_004983.1:n.-116A>T
|
|