ENST00000296684.10:c.182T>A
MANE Select
|
ENSP00000296684.5:p.Ile61Asn
|
|
ENST00000296684.9:c.182T>A
|
ENSP00000296684.5:p.Ile61Asn
|
|
ENST00000502423.5:c.*49T>A
|
ENSP00000422177.1:n.*49T>A
|
|
ENST00000506765.1:c.170T>A
|
ENSP00000424570.1:p.Ile57Asn
|
|
ENST00000506974.5:c.354T>A
|
ENSP00000425967.1:p.Tyr118Ter
|
|
ENST00000507026.5:c.*156T>A
|
ENSP00000424993.1:n.*156T>A
|
|
ENST00000509443.1:n.43T>A
|
|
|
NM_002495.2:c.182T>A
|
NP_002486.1:p.Ile61Asn
|
|
XM_005248525.3:c.182T>A
|
XP_005248582.1:p.Ile61Asn
|
|
XM_011543415.1:c.8T>A
|
XP_011541717.1:p.Ile3Asn
|
|
NM_001318051.1:c.182T>A
|
NP_001304980.1:p.Ile61Asn
|
|
NM_002495.3:c.182T>A
|
NP_002486.1:p.Ile61Asn
|
|
NR_134473.1:n.384T>A
|
|
|
NR_134474.1:n.301T>A
|
|
|
NR_134475.1:n.336T>A
|
|
|
NM_002495.4:c.182T>A
MANE Select
|
NP_002486.1:p.Ile61Asn
|
|
NM_001318051.2:c.182T>A
|
NP_001304980.1:p.Ile61Asn
|
|
NR_134473.2:n.378T>A
|
|
|
NR_134474.2:n.295T>A
|
|
|
NR_134475.2:n.330T>A
|
|
|