ENST00000456935.7:c.2777A>T
MANE Select
|
ENSP00000395473.2:p.Asp926Val
|
|
ENST00000221363.8:c.2774A>T
|
ENSP00000221363.4:p.Asp925Val
|
|
ENST00000456935.6:c.2777A>T
|
ENSP00000395473.2:p.Asp926Val
|
|
ENST00000466794.5:n.3367A>T
|
|
|
ENST00000469423.1:n.99A>T
|
|
|
ENST00000493218.5:n.188A>T
|
|
|
ENST00000597692.1:c.336A>T
|
|
|
NM_000528.3:c.2777A>T
|
NP_000519.2:p.Asp926Val
|
|
NM_001173498.1:c.2774A>T
|
NP_001166969.1:p.Asp925Val
|
|
XM_005259913.1:c.2780A>T
|
XP_005259970.1:p.Asp927Val
|
|
XM_011528017.1:c.1676A>T
|
XP_011526319.1:p.Asp559Val
|
|
XM_005259913.2:c.2780A>T
|
XP_005259970.1:p.Asp927Val
|
|
XM_024451518.1:c.1676A>T
|
XP_024307286.1:p.Asp559Val
|
|
NM_000528.4:c.2777A>T
MANE Select
|
NP_000519.2:p.Asp926Val
|
|
NM_001173498.2:c.2774A>T
|
NP_001166969.1:p.Asp925Val
|
|