ENST00000706989.1:c.1994G=
|
ENSP00000516702.1:p.Arg665=
|
|
ENST00000359125.7:c.1940G=
MANE Select
|
ENSP00000352035.2:p.Arg647=
|
|
ENST00000637193.1:c.1337G=
|
ENSP00000490734.1:p.Arg446=
|
|
ENST00000637338.1:n.97G=
|
|
|
ENST00000344462.8:c.1847G=
|
ENSP00000339611.4:p.Arg616=
|
|
ENST00000357249.6:c.1508G=
|
ENSP00000349789.3:p.Arg503=
|
|
ENST00000359125.6:c.1940G=
|
ENSP00000352035.2:p.Arg647=
|
|
ENST00000360480.7:c.1856G=
|
ENSP00000353668.3:p.Arg619=
|
|
ENST00000370224.5:c.1964G=
|
ENSP00000359244.2:p.Arg655=
|
|
ENST00000625514.2:c.1928G=
|
ENSP00000486040.1:p.Arg643=
|
|
ENST00000626839.2:c.1886G=
|
ENSP00000486706.1:p.Arg629=
|
|
ENST00000629241.2:c.1856G=
|
ENSP00000487142.1:p.Arg619=
|
|
ENST00000629676.2:c.1679+6127G=
|
ENSP00000486194.1:n.1679+6127G=
|
|
NM_004518.4:c.1856G=
|
NP_004509.2:p.Arg619=
|
|
NM_172106.1:c.1886G=
|
NP_742104.1:p.Arg629=
|
|
NM_172107.2:c.1940G=
|
NP_742105.1:p.Arg647=
|
|
NM_172108.3:c.1847G=
|
NP_742106.1:p.Arg616=
|
|
XM_006723787.1:c.1982G=
|
XP_006723850.1:p.Arg661=
|
|
XM_011528807.1:c.2048G=
|
XP_011527109.1:p.Arg683=
|
|
XM_011528808.1:c.2045G=
|
XP_011527110.1:p.Arg682=
|
|
XM_011528809.1:c.2018G=
|
XP_011527111.1:p.Arg673=
|
|
XM_011528810.1:c.1994G=
|
XP_011527112.1:p.Arg665=
|
|
XM_011528811.1:c.1964G=
|
XP_011527113.1:p.Arg655=
|
|
XM_011528812.1:c.1937G=
|
XP_011527114.1:p.Arg646=
|
|
XM_011528813.1:c.1922G=
|
XP_011527115.1:p.Arg641=
|
|
XM_011528814.1:c.1529G=
|
XP_011527116.1:p.Arg510=
|
|
NM_004518.5:c.1856G=
|
NP_004509.2:p.Arg619=
|
|
NM_172106.2:c.1886G=
|
NP_742104.1:p.Arg629=
|
|
NM_172107.3:c.1940G=
|
NP_742105.1:p.Arg647=
|
|
NM_172108.4:c.1847G=
|
NP_742106.1:p.Arg616=
|
|
XM_011528810.2:c.1994G=
|
XP_011527112.1:p.Arg665=
|
|
XM_011528811.2:c.1964G=
|
XP_011527113.1:p.Arg655=
|
|
XM_017027841.2:c.1991G=
|
XP_016883330.1:p.Arg664=
|
|
XM_017027842.2:c.1928G=
|
XP_016883331.1:p.Arg643=
|
|
XM_017027843.1:c.1925G=
|
XP_016883332.1:p.Arg642=
|
|
XM_017027844.2:c.1883G=
|
XP_016883333.1:p.Arg628=
|
|
XM_017027845.1:c.956G=
|
XP_016883334.1:p.Arg319=
|
|
NM_004518.6:c.1856G=
|
NP_004509.2:p.Arg619=
|
|
NM_172106.3:c.1886G=
|
NP_742104.1:p.Arg629=
|
|
NM_172107.4:c.1940G=
MANE Select
|
NP_742105.1:p.Arg647=
|
|
NM_172108.5:c.1847G=
|
NP_742106.1:p.Arg616=
|
|
NM_001382235.1:c.1994G=
|
NP_001369164.1:p.Arg665=
|
|