ENST00000706989.1:c.2104G=
|
ENSP00000516702.1:p.Gly702=
|
|
ENST00000359125.7:c.2050G=
MANE Select
|
ENSP00000352035.2:p.Gly684=
|
|
ENST00000637193.1:c.1447G=
|
ENSP00000490734.1:p.Gly483=
|
|
ENST00000344462.8:c.1957G=
|
ENSP00000339611.4:p.Gly653=
|
|
ENST00000357249.6:c.1618G=
|
ENSP00000349789.3:p.Gly540=
|
|
ENST00000359125.6:c.2050G=
|
ENSP00000352035.2:p.Gly684=
|
|
ENST00000360480.7:c.1966G=
|
ENSP00000353668.3:p.Gly656=
|
|
ENST00000370224.5:c.2074G=
|
ENSP00000359244.2:p.Gly692=
|
|
ENST00000625514.2:c.2038G=
|
ENSP00000486040.1:p.Gly680=
|
|
ENST00000626839.2:c.1996G=
|
ENSP00000486706.1:p.Gly666=
|
|
ENST00000629241.2:c.1966G=
|
ENSP00000487142.1:p.Gly656=
|
|
ENST00000629676.2:c.1679+6237G=
|
ENSP00000486194.1:n.1679+6237G=
|
|
NM_004518.4:c.1966G=
|
NP_004509.2:p.Gly656=
|
|
NM_172106.1:c.1996G=
|
NP_742104.1:p.Gly666=
|
|
NM_172107.2:c.2050G=
|
NP_742105.1:p.Gly684=
|
|
NM_172108.3:c.1957G=
|
NP_742106.1:p.Gly653=
|
|
XM_006723787.1:c.2092G=
|
XP_006723850.1:p.Gly698=
|
|
XM_011528807.1:c.2158G=
|
XP_011527109.1:p.Gly720=
|
|
XM_011528808.1:c.2155G=
|
XP_011527110.1:p.Gly719=
|
|
XM_011528809.1:c.2128G=
|
XP_011527111.1:p.Gly710=
|
|
XM_011528810.1:c.2104G=
|
XP_011527112.1:p.Gly702=
|
|
XM_011528811.1:c.2074G=
|
XP_011527113.1:p.Gly692=
|
|
XM_011528812.1:c.2047G=
|
XP_011527114.1:p.Gly683=
|
|
XM_011528813.1:c.2032G=
|
XP_011527115.1:p.Gly678=
|
|
XM_011528814.1:c.1639G=
|
XP_011527116.1:p.Gly547=
|
|
NM_004518.5:c.1966G=
|
NP_004509.2:p.Gly656=
|
|
NM_172106.2:c.1996G=
|
NP_742104.1:p.Gly666=
|
|
NM_172107.3:c.2050G=
|
NP_742105.1:p.Gly684=
|
|
NM_172108.4:c.1957G=
|
NP_742106.1:p.Gly653=
|
|
XM_011528810.2:c.2104G=
|
XP_011527112.1:p.Gly702=
|
|
XM_011528811.2:c.2074G=
|
XP_011527113.1:p.Gly692=
|
|
XM_017027841.2:c.2101G=
|
XP_016883330.1:p.Gly701=
|
|
XM_017027842.2:c.2038G=
|
XP_016883331.1:p.Gly680=
|
|
XM_017027843.1:c.2035G=
|
XP_016883332.1:p.Gly679=
|
|
XM_017027844.2:c.1993G=
|
XP_016883333.1:p.Gly665=
|
|
XM_017027845.1:c.1066G=
|
XP_016883334.1:p.Gly356=
|
|
NM_004518.6:c.1966G=
|
NP_004509.2:p.Gly656=
|
|
NM_172106.3:c.1996G=
|
NP_742104.1:p.Gly666=
|
|
NM_172107.4:c.2050G=
MANE Select
|
NP_742105.1:p.Gly684=
|
|
NM_172108.5:c.1957G=
|
NP_742106.1:p.Gly653=
|
|
NM_001382235.1:c.2104G=
|
NP_001369164.1:p.Gly702=
|
|