ENST00000706989.1:c.2125C>G
|
ENSP00000516702.1:p.Arg709Gly
|
|
ENST00000359125.7:c.2071C>G
MANE Select
|
ENSP00000352035.2:p.Arg691Gly
|
|
ENST00000637193.1:c.1468C>G
|
ENSP00000490734.1:p.Arg490Gly
|
|
ENST00000344462.8:c.1978C>G
|
ENSP00000339611.4:p.Arg660Gly
|
|
ENST00000357249.6:c.1639C>G
|
ENSP00000349789.3:p.Arg547Gly
|
|
ENST00000359125.6:c.2071C>G
|
ENSP00000352035.2:p.Arg691Gly
|
|
ENST00000360480.7:c.1987C>G
|
ENSP00000353668.3:p.Arg663Gly
|
|
ENST00000370224.5:c.2095C>G
|
ENSP00000359244.2:p.Arg699Gly
|
|
ENST00000625514.2:c.2059C>G
|
ENSP00000486040.1:p.Arg687Gly
|
|
ENST00000626839.2:c.2017C>G
|
ENSP00000486706.1:p.Arg673Gly
|
|
ENST00000629241.2:c.1987C>G
|
ENSP00000487142.1:p.Arg663Gly
|
|
ENST00000629676.2:c.1679+6258C>G
|
ENSP00000486194.1:n.1679+6258C>G
|
|
NM_004518.4:c.1987C>G
|
NP_004509.2:p.Arg663Gly
|
|
NM_172106.1:c.2017C>G
|
NP_742104.1:p.Arg673Gly
|
|
NM_172107.2:c.2071C>G
|
NP_742105.1:p.Arg691Gly
|
|
NM_172108.3:c.1978C>G
|
NP_742106.1:p.Arg660Gly
|
|
XM_006723787.1:c.2113C>G
|
XP_006723850.1:p.Arg705Gly
|
|
XM_011528807.1:c.2179C>G
|
XP_011527109.1:p.Arg727Gly
|
|
XM_011528808.1:c.2176C>G
|
XP_011527110.1:p.Arg726Gly
|
|
XM_011528809.1:c.2149C>G
|
XP_011527111.1:p.Arg717Gly
|
|
XM_011528810.1:c.2125C>G
|
XP_011527112.1:p.Arg709Gly
|
|
XM_011528811.1:c.2095C>G
|
XP_011527113.1:p.Arg699Gly
|
|
XM_011528812.1:c.2068C>G
|
XP_011527114.1:p.Arg690Gly
|
|
XM_011528813.1:c.2053C>G
|
XP_011527115.1:p.Arg685Gly
|
|
XM_011528814.1:c.1660C>G
|
XP_011527116.1:p.Arg554Gly
|
|
NM_004518.5:c.1987C>G
|
NP_004509.2:p.Arg663Gly
|
|
NM_172106.2:c.2017C>G
|
NP_742104.1:p.Arg673Gly
|
|
NM_172107.3:c.2071C>G
|
NP_742105.1:p.Arg691Gly
|
|
NM_172108.4:c.1978C>G
|
NP_742106.1:p.Arg660Gly
|
|
XM_011528810.2:c.2125C>G
|
XP_011527112.1:p.Arg709Gly
|
|
XM_011528811.2:c.2095C>G
|
XP_011527113.1:p.Arg699Gly
|
|
XM_017027841.2:c.2122C>G
|
XP_016883330.1:p.Arg708Gly
|
|
XM_017027842.2:c.2059C>G
|
XP_016883331.1:p.Arg687Gly
|
|
XM_017027843.1:c.2056C>G
|
XP_016883332.1:p.Arg686Gly
|
|
XM_017027844.2:c.2014C>G
|
XP_016883333.1:p.Arg672Gly
|
|
XM_017027845.1:c.1087C>G
|
XP_016883334.1:p.Arg363Gly
|
|
NM_004518.6:c.1987C>G
|
NP_004509.2:p.Arg663Gly
|
|
NM_172106.3:c.2017C>G
|
NP_742104.1:p.Arg673Gly
|
|
NM_172107.4:c.2071C>G
MANE Select
|
NP_742105.1:p.Arg691Gly
|
|
NM_172108.5:c.1978C>G
|
NP_742106.1:p.Arg660Gly
|
|
NM_001382235.1:c.2125C>G
|
NP_001369164.1:p.Arg709Gly
|
|