ENST00000456935.7:c.2859G>C
MANE Select
|
ENSP00000395473.2:p.Glu953Asp
|
|
ENST00000221363.8:c.2856G>C
|
ENSP00000221363.4:p.Glu952Asp
|
|
ENST00000456935.6:c.2859G>C
|
ENSP00000395473.2:p.Glu953Asp
|
|
ENST00000466794.5:n.3449G>C
|
|
|
ENST00000469423.1:n.288G>C
|
|
|
ENST00000493218.5:n.270G>C
|
|
|
ENST00000597692.1:c.418G>C
|
|
|
NM_000528.3:c.2859G>C
|
NP_000519.2:p.Glu953Asp
|
|
NM_001173498.1:c.2856G>C
|
NP_001166969.1:p.Glu952Asp
|
|
XM_005259913.1:c.2862G>C
|
XP_005259970.1:p.Glu954Asp
|
|
XM_011528017.1:c.1758G>C
|
XP_011526319.1:p.Glu586Asp
|
|
XM_005259913.2:c.2862G>C
|
XP_005259970.1:p.Glu954Asp
|
|
XM_024451518.1:c.1758G>C
|
XP_024307286.1:p.Glu586Asp
|
|
NM_000528.4:c.2859G>C
MANE Select
|
NP_000519.2:p.Glu953Asp
|
|
NM_001173498.2:c.2856G>C
|
NP_001166969.1:p.Glu952Asp
|
|