ENST00000706989.1:c.2313C>G
|
ENSP00000516702.1:p.Ser771=
|
|
ENST00000359125.7:c.2259C>G
MANE Select
|
ENSP00000352035.2:p.Ser753=
|
|
ENST00000637193.1:c.1656C>G
|
ENSP00000490734.1:p.Ser552=
|
|
ENST00000344462.8:c.2166C>G
|
ENSP00000339611.4:p.Ser722=
|
|
ENST00000357249.6:c.1827C>G
|
ENSP00000349789.3:p.Ser609=
|
|
ENST00000359125.6:c.2259C>G
|
ENSP00000352035.2:p.Ser753=
|
|
ENST00000360480.7:c.2175C>G
|
ENSP00000353668.3:p.Ser725=
|
|
ENST00000370224.5:c.2241+42C>G
|
ENSP00000359244.2:n.2241+42C>G
|
|
ENST00000625514.2:c.2205+42C>G
|
ENSP00000486040.1:n.2205+42C>G
|
|
ENST00000626839.2:c.2205C>G
|
ENSP00000486706.1:p.Ser735=
|
|
ENST00000629241.2:c.2133+42C>G
|
ENSP00000487142.1:n.2133+42C>G
|
|
ENST00000629676.2:c.1680-6161C>G
|
ENSP00000486194.1:n.1680-6161C>G
|
|
NM_004518.4:c.2175C>G
|
NP_004509.2:p.Ser725=
|
|
NM_172106.1:c.2205C>G
|
NP_742104.1:p.Ser735=
|
|
NM_172107.2:c.2259C>G
|
NP_742105.1:p.Ser753=
|
|
NM_172108.3:c.2166C>G
|
NP_742106.1:p.Ser722=
|
|
XM_006723787.1:c.2301C>G
|
XP_006723850.1:p.Ser767=
|
|
XM_011528807.1:c.2367C>G
|
XP_011527109.1:p.Ser789=
|
|
XM_011528808.1:c.2364C>G
|
XP_011527110.1:p.Ser788=
|
|
XM_011528809.1:c.2337C>G
|
XP_011527111.1:p.Ser779=
|
|
XM_011528810.1:c.2313C>G
|
XP_011527112.1:p.Ser771=
|
|
XM_011528811.1:c.2283C>G
|
XP_011527113.1:p.Ser761=
|
|
XM_011528812.1:c.2256C>G
|
XP_011527114.1:p.Ser752=
|
|
XM_011528813.1:c.2241C>G
|
XP_011527115.1:p.Ser747=
|
|
XM_011528814.1:c.1848C>G
|
XP_011527116.1:p.Ser616=
|
|
NM_004518.5:c.2175C>G
|
NP_004509.2:p.Ser725=
|
|
NM_172106.2:c.2205C>G
|
NP_742104.1:p.Ser735=
|
|
NM_172107.3:c.2259C>G
|
NP_742105.1:p.Ser753=
|
|
NM_172108.4:c.2166C>G
|
NP_742106.1:p.Ser722=
|
|
XM_011528810.2:c.2313C>G
|
XP_011527112.1:p.Ser771=
|
|
XM_011528811.2:c.2283C>G
|
XP_011527113.1:p.Ser761=
|
|
XM_017027841.2:c.2310C>G
|
XP_016883330.1:p.Ser770=
|
|
XM_017027842.2:c.2247C>G
|
XP_016883331.1:p.Ser749=
|
|
XM_017027843.1:c.2244C>G
|
XP_016883332.1:p.Ser748=
|
|
XM_017027844.2:c.2202C>G
|
XP_016883333.1:p.Ser734=
|
|
XM_017027845.1:c.1275C>G
|
XP_016883334.1:p.Ser425=
|
|
NM_004518.6:c.2175C>G
|
NP_004509.2:p.Ser725=
|
|
NM_172106.3:c.2205C>G
|
NP_742104.1:p.Ser735=
|
|
NM_172107.4:c.2259C>G
MANE Select
|
NP_742105.1:p.Ser753=
|
|
NM_172108.5:c.2166C>G
|
NP_742106.1:p.Ser722=
|
|
NM_001382235.1:c.2313C>G
|
NP_001369164.1:p.Ser771=
|
|