ENST00000296684.10:c.400G>T
MANE Select
|
ENSP00000296684.5:p.Ala134Ser
|
|
ENST00000296684.9:c.400G>T
|
ENSP00000296684.5:p.Ala134Ser
|
|
ENST00000502423.5:c.*267G>T
|
ENSP00000422177.1:n.*267G>T
|
|
ENST00000506765.1:c.338+12195G>T
|
ENSP00000424570.1:n.338+12195G>T
|
|
ENST00000506974.5:c.*176G>T
|
ENSP00000425967.1:n.*176G>T
|
|
ENST00000507026.5:c.*374G>T
|
ENSP00000424993.1:n.*374G>T
|
|
ENST00000509443.1:n.261G>T
|
|
|
NM_002495.2:c.400G>T
|
NP_002486.1:p.Ala134Ser
|
|
XM_005248525.3:c.350+12195G>T
|
XP_005248582.1:n.350+12195G>T
|
|
XM_011543415.1:c.226G>T
|
XP_011541717.1:p.Ala76Ser
|
|
NM_001318051.1:c.350+12195G>T
|
NP_001304980.1:n.350+12195G>T
|
|
NM_002495.3:c.400G>T
|
NP_002486.1:p.Ala134Ser
|
|
NR_134473.1:n.602G>T
|
|
|
NR_134474.1:n.519G>T
|
|
|
NR_134475.1:n.554G>T
|
|
|
NM_002495.4:c.400G>T
MANE Select
|
NP_002486.1:p.Ala134Ser
|
|
NM_001318051.2:c.350+12195G>T
|
NP_001304980.1:n.350+12195G>T
|
|
NR_134473.2:n.596G>T
|
|
|
NR_134474.2:n.513G>T
|
|
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NR_134475.2:n.548G>T
|
|
|