|
NM_053017.5:c.466G>A
MANE Select
|
NP_443750.2:p.Glu156Lys
|
|
ENST00000397068.8:c.466G>A
MANE Select
|
ENSP00000380258.3:p.Glu156Lys
|
|
NM_001079536.1:c.466G>A
|
NP_001073004.1:p.Glu156Lys
|
|
NM_001079536.2:c.466G>A
|
NP_001073004.1:p.Glu156Lys
|
|
NM_001297668.1:c.466G>A
|
NP_001284597.1:p.Glu156Lys
|
|
NM_001297668.2:c.466G>A
|
NP_001284597.1:p.Glu156Lys
|
|
NM_053017.4:c.466G>A
|
NP_443750.2:p.Glu156Lys
|
|
NR_123732.1:n.140-168G>A
|
|
|
NR_123732.2:n.203-168G>A
|
|
|
ENST00000359918.8:c.466G>A
|
ENSP00000352992.4:p.Glu156Lys
|
|
ENST00000397067.7:c.466G>A
|
ENSP00000380257.3:p.Glu156Lys
|
|
ENST00000397068.7:c.466G>A
|
ENSP00000380258.3:p.Glu156Lys
|
|
ENST00000425767.2:c.276+127G>A
|
ENSP00000413852.2:n.276+127G>A
|
|
ENST00000453353.2:c.335G>A
|
|
|
XM_005252779.2:c.466G>A
|
XP_005252836.1:p.Glu156Lys
|
|
XM_005252779.3:c.466G>A
|
XP_005252836.1:p.Glu156Lys
|
|
XM_005252780.2:c.466G>A
|
XP_005252837.1:p.Glu156Lys
|
|
XM_006718136.2:c.466G>A
|
XP_006718199.1:p.Glu156Lys
|
|
XM_006718136.4:c.466G>A
|
XP_006718199.1:p.Glu156Lys
|
|
XM_006718137.2:c.466G>A
|
XP_006718200.1:p.Glu156Lys
|
|
XM_011519879.1:c.466G>A
|
XP_011518181.1:p.Glu156Lys
|
|
XM_011519879.3:c.466G>A
|
XP_011518181.1:p.Glu156Lys
|
|
XM_011519880.1:c.466G>A
|
XP_011518182.1:p.Glu156Lys
|
|
XM_017017171.1:c.58-168G>A
|
XP_016872660.1:n.58-168G>A
|