ENST00000288774.8:c.944A>T
|
ENSP00000288774.3:p.Glu315Val
|
|
ENST00000447513.7:c.884A>T
MANE Select
|
ENSP00000407922.2:p.Glu295Val
|
|
ENST00000650293.1:c.838A>T
|
|
|
ENST00000288774.7:c.944A>T
|
ENSP00000288774.3:p.Glu315Val
|
|
ENST00000447513.6:c.884A>T
|
ENSP00000407922.2:p.Glu295Val
|
|
ENST00000507596.5:c.884A>T
|
ENSP00000424291.1:p.Glu295Val
|
|
NM_002617.3:c.884A>T
|
NP_002608.1:p.Glu295Val
|
|
NM_153818.1:c.944A>T
|
NP_722540.1:p.Glu315Val
|
|
XM_011541573.1:c.941A>T
|
XP_011539875.1:p.Glu314Val
|
|
XM_011541574.1:c.509A>T
|
XP_011539876.1:p.Glu170Val
|
|
XM_011541575.1:c.509A>T
|
XP_011539877.1:p.Glu170Val
|
|
XR_946666.1:n.1000A>T
|
|
|
XR_946666.2:n.949A>T
|
|
|
NM_001374425.1:c.941A>T
|
NP_001361354.1:p.Glu314Val
|
|
NM_001374426.1:c.509A>T
|
NP_001361355.1:p.Glu170Val
|
|
NM_001374427.1:c.452A>T
|
NP_001361356.1:p.Glu151Val
|
|
NM_002617.4:c.884A>T
MANE Select
|
NP_002608.1:p.Glu295Val
|
|
NM_153818.2:c.944A>T
|
NP_722540.1:p.Glu315Val
|
|
NR_164636.1:n.999A>T
|
|
|