ENST00000706989.1:c.2160G=
|
ENSP00000516702.1:p.Ser720=
|
|
ENST00000359125.7:c.2106G=
MANE Select
|
ENSP00000352035.2:p.Ser702=
|
|
ENST00000637193.1:c.1503G=
|
ENSP00000490734.1:p.Ser501=
|
|
ENST00000344462.8:c.2013G=
|
ENSP00000339611.4:p.Ser671=
|
|
ENST00000357249.6:c.1674G=
|
ENSP00000349789.3:p.Ser558=
|
|
ENST00000359125.6:c.2106G=
|
ENSP00000352035.2:p.Ser702=
|
|
ENST00000360480.7:c.2022G=
|
ENSP00000353668.3:p.Ser674=
|
|
ENST00000370224.5:c.2130G=
|
ENSP00000359244.2:p.Ser710=
|
|
ENST00000625514.2:c.2094G=
|
ENSP00000486040.1:p.Ser698=
|
|
ENST00000626839.2:c.2052G=
|
ENSP00000486706.1:p.Ser684=
|
|
ENST00000629241.2:c.2022G=
|
ENSP00000487142.1:p.Ser674=
|
|
ENST00000629676.2:c.1679+6293G=
|
ENSP00000486194.1:n.1679+6293G=
|
|
NM_004518.4:c.2022G=
|
NP_004509.2:p.Ser674=
|
|
NM_172106.1:c.2052G=
|
NP_742104.1:p.Ser684=
|
|
NM_172107.2:c.2106G=
|
NP_742105.1:p.Ser702=
|
|
NM_172108.3:c.2013G=
|
NP_742106.1:p.Ser671=
|
|
XM_006723787.1:c.2148G=
|
XP_006723850.1:p.Ser716=
|
|
XM_011528807.1:c.2214G=
|
XP_011527109.1:p.Ser738=
|
|
XM_011528808.1:c.2211G=
|
XP_011527110.1:p.Ser737=
|
|
XM_011528809.1:c.2184G=
|
XP_011527111.1:p.Ser728=
|
|
XM_011528810.1:c.2160G=
|
XP_011527112.1:p.Ser720=
|
|
XM_011528811.1:c.2130G=
|
XP_011527113.1:p.Ser710=
|
|
XM_011528812.1:c.2103G=
|
XP_011527114.1:p.Ser701=
|
|
XM_011528813.1:c.2088G=
|
XP_011527115.1:p.Ser696=
|
|
XM_011528814.1:c.1695G=
|
XP_011527116.1:p.Ser565=
|
|
NM_004518.5:c.2022G=
|
NP_004509.2:p.Ser674=
|
|
NM_172106.2:c.2052G=
|
NP_742104.1:p.Ser684=
|
|
NM_172107.3:c.2106G=
|
NP_742105.1:p.Ser702=
|
|
NM_172108.4:c.2013G=
|
NP_742106.1:p.Ser671=
|
|
XM_011528810.2:c.2160G=
|
XP_011527112.1:p.Ser720=
|
|
XM_011528811.2:c.2130G=
|
XP_011527113.1:p.Ser710=
|
|
XM_017027841.2:c.2157G=
|
XP_016883330.1:p.Ser719=
|
|
XM_017027842.2:c.2094G=
|
XP_016883331.1:p.Ser698=
|
|
XM_017027843.1:c.2091G=
|
XP_016883332.1:p.Ser697=
|
|
XM_017027844.2:c.2049G=
|
XP_016883333.1:p.Ser683=
|
|
XM_017027845.1:c.1122G=
|
XP_016883334.1:p.Ser374=
|
|
NM_004518.6:c.2022G=
|
NP_004509.2:p.Ser674=
|
|
NM_172106.3:c.2052G=
|
NP_742104.1:p.Ser684=
|
|
NM_172107.4:c.2106G=
MANE Select
|
NP_742105.1:p.Ser702=
|
|
NM_172108.5:c.2013G=
|
NP_742106.1:p.Ser671=
|
|
NM_001382235.1:c.2160G=
|
NP_001369164.1:p.Ser720=
|
|