ENST00000342245.9:c.1345G>A
MANE Select
|
ENSP00000340409.4:p.Glu449Lys
|
|
ENST00000342245.8:c.1345G>A
|
ENSP00000340409.4:p.Glu449Lys
|
|
ENST00000526280.1:c.402G>A
|
|
|
ENST00000527275.5:c.1342G>A
|
ENSP00000435350.1:p.Glu448Lys
|
|
ENST00000531303.5:c.*176G>A
|
ENSP00000432625.1:n.*176G>A
|
|
ENST00000531336.1:n.177G>A
|
|
|
ENST00000532367.1:n.181G>A
|
|
|
ENST00000533123.5:c.*72G>A
|
ENSP00000435950.1:n.*72G>A
|
|
ENST00000534405.5:c.*176G>A
|
ENSP00000434353.1:n.*176G>A
|
|
NM_000543.4:c.1345G>A
|
NP_000534.3:p.Glu449Lys
|
|
NM_001007593.2:c.1342G>A
|
NP_001007594.2:p.Glu448Lys
|
|
XM_005253075.3:c.1345G>A
|
XP_005253132.1:p.Glu449Lys
|
|
XM_011520303.1:c.1213G>A
|
XP_011518605.1:p.Glu405Lys
|
|
XM_011520304.1:c.1213G>A
|
XP_011518606.1:p.Glu405Lys
|
|
XR_930886.1:n.1683G>A
|
|
|
NM_001318087.1:c.1345G>A
|
NP_001305016.1:p.Glu449Lys
|
|
NM_001318088.1:c.424G>A
|
NP_001305017.1:p.Glu142Lys
|
|
NM_001365135.1:c.1213G>A
|
NP_001352064.1:p.Glu405Lys
|
|
NR_027400.2:n.1358G>A
|
|
|
NR_134502.1:n.877G>A
|
|
|
XM_011520304.2:c.1213G>A
|
XP_011518606.1:p.Glu405Lys
|
|
XR_001747940.2:n.1510G>A
|
|
|
XR_002957158.1:n.1712G>A
|
|
|
NM_000543.5:c.1345G>A
MANE Select
|
NP_000534.3:p.Glu449Lys
|
|
NM_001007593.3:c.1342G>A
|
NP_001007594.2:p.Glu448Lys
|
|
NM_001318087.2:c.1345G>A
|
NP_001305016.1:p.Glu449Lys
|
|
NM_001318088.2:c.424G>A
|
NP_001305017.1:p.Glu142Lys
|
|
NM_001365135.2:c.1213G>A
|
NP_001352064.1:p.Glu405Lys
|
|
NR_027400.3:n.1298G>A
|
|
|
NR_134502.2:n.817G>A
|
|
|