ENST00000296684.10:c.367A>T
MANE Select
|
ENSP00000296684.5:p.Asn123Tyr
|
|
ENST00000296684.9:c.367A>T
|
ENSP00000296684.5:p.Asn123Tyr
|
|
ENST00000502423.5:c.*234A>T
|
ENSP00000422177.1:n.*234A>T
|
|
ENST00000506765.1:c.338+12162A>T
|
ENSP00000424570.1:n.338+12162A>T
|
|
ENST00000506974.5:c.*143A>T
|
ENSP00000425967.1:n.*143A>T
|
|
ENST00000507026.5:c.*341A>T
|
ENSP00000424993.1:n.*341A>T
|
|
ENST00000509443.1:n.228A>T
|
|
|
NM_002495.2:c.367A>T
|
NP_002486.1:p.Asn123Tyr
|
|
XM_005248525.3:c.350+12162A>T
|
XP_005248582.1:n.350+12162A>T
|
|
XM_011543415.1:c.193A>T
|
XP_011541717.1:p.Asn65Tyr
|
|
NM_001318051.1:c.350+12162A>T
|
NP_001304980.1:n.350+12162A>T
|
|
NM_002495.3:c.367A>T
|
NP_002486.1:p.Asn123Tyr
|
|
NR_134473.1:n.569A>T
|
|
|
NR_134474.1:n.486A>T
|
|
|
NR_134475.1:n.521A>T
|
|
|
NM_002495.4:c.367A>T
MANE Select
|
NP_002486.1:p.Asn123Tyr
|
|
NM_001318051.2:c.350+12162A>T
|
NP_001304980.1:n.350+12162A>T
|
|
NR_134473.2:n.563A>T
|
|
|
NR_134474.2:n.480A>T
|
|
|
NR_134475.2:n.515A>T
|
|
|