ENST00000706989.1:c.2394C>T
|
ENSP00000516702.1:p.Asn798=
|
|
ENST00000359125.7:c.2340C>T
MANE Select
|
ENSP00000352035.2:p.Asn780=
|
|
ENST00000637193.1:c.1737C>T
|
ENSP00000490734.1:p.Asn579=
|
|
ENST00000344462.8:c.2247C>T
|
ENSP00000339611.4:p.Asn749=
|
|
ENST00000357249.6:c.1908C>T
|
ENSP00000349789.3:p.Asn636=
|
|
ENST00000359125.6:c.2340C>T
|
ENSP00000352035.2:p.Asn780=
|
|
ENST00000360480.7:c.2256C>T
|
ENSP00000353668.3:p.Asn752=
|
|
ENST00000370224.5:c.2241+123C>T
|
ENSP00000359244.2:n.2241+123C>T
|
|
ENST00000625514.2:c.2205+123C>T
|
ENSP00000486040.1:n.2205+123C>T
|
|
ENST00000626839.2:c.2286C>T
|
ENSP00000486706.1:p.Asn762=
|
|
ENST00000629241.2:c.2133+123C>T
|
ENSP00000487142.1:n.2133+123C>T
|
|
ENST00000629676.2:c.1680-6080C>T
|
ENSP00000486194.1:n.1680-6080C>T
|
|
NM_004518.4:c.2256C>T
|
NP_004509.2:p.Asn752=
|
|
NM_172106.1:c.2286C>T
|
NP_742104.1:p.Asn762=
|
|
NM_172107.2:c.2340C>T
|
NP_742105.1:p.Asn780=
|
|
NM_172108.3:c.2247C>T
|
NP_742106.1:p.Asn749=
|
|
XM_006723787.1:c.2382C>T
|
XP_006723850.1:p.Asn794=
|
|
XM_011528807.1:c.2448C>T
|
XP_011527109.1:p.Asn816=
|
|
XM_011528808.1:c.2445C>T
|
XP_011527110.1:p.Asn815=
|
|
XM_011528809.1:c.2418C>T
|
XP_011527111.1:p.Asn806=
|
|
XM_011528810.1:c.2394C>T
|
XP_011527112.1:p.Asn798=
|
|
XM_011528811.1:c.2364C>T
|
XP_011527113.1:p.Asn788=
|
|
XM_011528812.1:c.2337C>T
|
XP_011527114.1:p.Asn779=
|
|
XM_011528813.1:c.2322C>T
|
XP_011527115.1:p.Asn774=
|
|
XM_011528814.1:c.1929C>T
|
XP_011527116.1:p.Asn643=
|
|
NM_004518.5:c.2256C>T
|
NP_004509.2:p.Asn752=
|
|
NM_172106.2:c.2286C>T
|
NP_742104.1:p.Asn762=
|
|
NM_172107.3:c.2340C>T
|
NP_742105.1:p.Asn780=
|
|
NM_172108.4:c.2247C>T
|
NP_742106.1:p.Asn749=
|
|
XM_011528810.2:c.2394C>T
|
XP_011527112.1:p.Asn798=
|
|
XM_011528811.2:c.2364C>T
|
XP_011527113.1:p.Asn788=
|
|
XM_017027841.2:c.2391C>T
|
XP_016883330.1:p.Asn797=
|
|
XM_017027842.2:c.2328C>T
|
XP_016883331.1:p.Asn776=
|
|
XM_017027843.1:c.2325C>T
|
XP_016883332.1:p.Asn775=
|
|
XM_017027844.2:c.2283C>T
|
XP_016883333.1:p.Asn761=
|
|
XM_017027845.1:c.1356C>T
|
XP_016883334.1:p.Asn452=
|
|
NM_004518.6:c.2256C>T
|
NP_004509.2:p.Asn752=
|
|
NM_172106.3:c.2286C>T
|
NP_742104.1:p.Asn762=
|
|
NM_172107.4:c.2340C>T
MANE Select
|
NP_742105.1:p.Asn780=
|
|
NM_172108.5:c.2247C>T
|
NP_742106.1:p.Asn749=
|
|
NM_001382235.1:c.2394C>T
|
NP_001369164.1:p.Asn798=
|
|