ENST00000706989.1:c.2077G>C
|
ENSP00000516702.1:p.Asp693His
|
|
ENST00000359125.7:c.2023G>C
MANE Select
|
ENSP00000352035.2:p.Asp675His
|
|
ENST00000637193.1:c.1420G>C
|
ENSP00000490734.1:p.Asp474His
|
|
ENST00000344462.8:c.1930G>C
|
ENSP00000339611.4:p.Asp644His
|
|
ENST00000357249.6:c.1591G>C
|
ENSP00000349789.3:p.Asp531His
|
|
ENST00000359125.6:c.2023G>C
|
ENSP00000352035.2:p.Asp675His
|
|
ENST00000360480.7:c.1939G>C
|
ENSP00000353668.3:p.Asp647His
|
|
ENST00000370224.5:c.2047G>C
|
ENSP00000359244.2:p.Asp683His
|
|
ENST00000625514.2:c.2011G>C
|
ENSP00000486040.1:p.Asp671His
|
|
ENST00000626839.2:c.1969G>C
|
ENSP00000486706.1:p.Asp657His
|
|
ENST00000629241.2:c.1939G>C
|
ENSP00000487142.1:p.Asp647His
|
|
ENST00000629676.2:c.1679+6210G>C
|
ENSP00000486194.1:n.1679+6210G>C
|
|
NM_004518.4:c.1939G>C
|
NP_004509.2:p.Asp647His
|
|
NM_172106.1:c.1969G>C
|
NP_742104.1:p.Asp657His
|
|
NM_172107.2:c.2023G>C
|
NP_742105.1:p.Asp675His
|
|
NM_172108.3:c.1930G>C
|
NP_742106.1:p.Asp644His
|
|
XM_006723787.1:c.2065G>C
|
XP_006723850.1:p.Asp689His
|
|
XM_011528807.1:c.2131G>C
|
XP_011527109.1:p.Asp711His
|
|
XM_011528808.1:c.2128G>C
|
XP_011527110.1:p.Asp710His
|
|
XM_011528809.1:c.2101G>C
|
XP_011527111.1:p.Asp701His
|
|
XM_011528810.1:c.2077G>C
|
XP_011527112.1:p.Asp693His
|
|
XM_011528811.1:c.2047G>C
|
XP_011527113.1:p.Asp683His
|
|
XM_011528812.1:c.2020G>C
|
XP_011527114.1:p.Asp674His
|
|
XM_011528813.1:c.2005G>C
|
XP_011527115.1:p.Asp669His
|
|
XM_011528814.1:c.1612G>C
|
XP_011527116.1:p.Asp538His
|
|
NM_004518.5:c.1939G>C
|
NP_004509.2:p.Asp647His
|
|
NM_172106.2:c.1969G>C
|
NP_742104.1:p.Asp657His
|
|
NM_172107.3:c.2023G>C
|
NP_742105.1:p.Asp675His
|
|
NM_172108.4:c.1930G>C
|
NP_742106.1:p.Asp644His
|
|
XM_011528810.2:c.2077G>C
|
XP_011527112.1:p.Asp693His
|
|
XM_011528811.2:c.2047G>C
|
XP_011527113.1:p.Asp683His
|
|
XM_017027841.2:c.2074G>C
|
XP_016883330.1:p.Asp692His
|
|
XM_017027842.2:c.2011G>C
|
XP_016883331.1:p.Asp671His
|
|
XM_017027843.1:c.2008G>C
|
XP_016883332.1:p.Asp670His
|
|
XM_017027844.2:c.1966G>C
|
XP_016883333.1:p.Asp656His
|
|
XM_017027845.1:c.1039G>C
|
XP_016883334.1:p.Asp347His
|
|
NM_004518.6:c.1939G>C
|
NP_004509.2:p.Asp647His
|
|
NM_172106.3:c.1969G>C
|
NP_742104.1:p.Asp657His
|
|
NM_172107.4:c.2023G>C
MANE Select
|
NP_742105.1:p.Asp675His
|
|
NM_172108.5:c.1930G>C
|
NP_742106.1:p.Asp644His
|
|
NM_001382235.1:c.2077G>C
|
NP_001369164.1:p.Asp693His
|
|