ENST00000706989.1:c.2306C=
|
ENSP00000516702.1:p.Ser769=
|
|
ENST00000359125.7:c.2252C=
MANE Select
|
ENSP00000352035.2:p.Ser751=
|
|
ENST00000637193.1:c.1649C=
|
ENSP00000490734.1:p.Ser550=
|
|
ENST00000344462.8:c.2159C=
|
ENSP00000339611.4:p.Ser720=
|
|
ENST00000357249.6:c.1820C=
|
ENSP00000349789.3:p.Ser607=
|
|
ENST00000359125.6:c.2252C=
|
ENSP00000352035.2:p.Ser751=
|
|
ENST00000360480.7:c.2168C=
|
ENSP00000353668.3:p.Ser723=
|
|
ENST00000370224.5:c.2241+35C=
|
ENSP00000359244.2:n.2241+35C=
|
|
ENST00000625514.2:c.2205+35C=
|
ENSP00000486040.1:n.2205+35C=
|
|
ENST00000626839.2:c.2198C=
|
ENSP00000486706.1:p.Ser733=
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|
ENST00000629241.2:c.2133+35C=
|
ENSP00000487142.1:n.2133+35C=
|
|
ENST00000629676.2:c.1680-6168C=
|
ENSP00000486194.1:n.1680-6168C=
|
|
NM_004518.4:c.2168C=
|
NP_004509.2:p.Ser723=
|
|
NM_172106.1:c.2198C=
|
NP_742104.1:p.Ser733=
|
|
NM_172107.2:c.2252C=
|
NP_742105.1:p.Ser751=
|
|
NM_172108.3:c.2159C=
|
NP_742106.1:p.Ser720=
|
|
XM_006723787.1:c.2294C=
|
XP_006723850.1:p.Ser765=
|
|
XM_011528807.1:c.2360C=
|
XP_011527109.1:p.Ser787=
|
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XM_011528808.1:c.2357C=
|
XP_011527110.1:p.Ser786=
|
|
XM_011528809.1:c.2330C=
|
XP_011527111.1:p.Ser777=
|
|
XM_011528810.1:c.2306C=
|
XP_011527112.1:p.Ser769=
|
|
XM_011528811.1:c.2276C=
|
XP_011527113.1:p.Ser759=
|
|
XM_011528812.1:c.2249C=
|
XP_011527114.1:p.Ser750=
|
|
XM_011528813.1:c.2234C=
|
XP_011527115.1:p.Ser745=
|
|
XM_011528814.1:c.1841C=
|
XP_011527116.1:p.Ser614=
|
|
NM_004518.5:c.2168C=
|
NP_004509.2:p.Ser723=
|
|
NM_172106.2:c.2198C=
|
NP_742104.1:p.Ser733=
|
|
NM_172107.3:c.2252C=
|
NP_742105.1:p.Ser751=
|
|
NM_172108.4:c.2159C=
|
NP_742106.1:p.Ser720=
|
|
XM_011528810.2:c.2306C=
|
XP_011527112.1:p.Ser769=
|
|
XM_011528811.2:c.2276C=
|
XP_011527113.1:p.Ser759=
|
|
XM_017027841.2:c.2303C=
|
XP_016883330.1:p.Ser768=
|
|
XM_017027842.2:c.2240C=
|
XP_016883331.1:p.Ser747=
|
|
XM_017027843.1:c.2237C=
|
XP_016883332.1:p.Ser746=
|
|
XM_017027844.2:c.2195C=
|
XP_016883333.1:p.Ser732=
|
|
XM_017027845.1:c.1268C=
|
XP_016883334.1:p.Ser423=
|
|
NM_004518.6:c.2168C=
|
NP_004509.2:p.Ser723=
|
|
NM_172106.3:c.2198C=
|
NP_742104.1:p.Ser733=
|
|
NM_172107.4:c.2252C=
MANE Select
|
NP_742105.1:p.Ser751=
|
|
NM_172108.5:c.2159C=
|
NP_742106.1:p.Ser720=
|
|
NM_001382235.1:c.2306C=
|
NP_001369164.1:p.Ser769=
|
|