ENST00000706989.1:c.1677C>T
|
ENSP00000516702.1:p.Asp559=
|
|
ENST00000359125.7:c.1731C>T
MANE Select
|
ENSP00000352035.2:p.Asp577=
|
|
ENST00000637193.1:c.1128C>T
|
ENSP00000490734.1:p.Asp376=
|
|
ENST00000344462.8:c.1638C>T
|
ENSP00000339611.4:p.Asp546=
|
|
ENST00000357249.6:c.1299C>T
|
ENSP00000349789.3:p.Asp433=
|
|
ENST00000359125.6:c.1731C>T
|
ENSP00000352035.2:p.Asp577=
|
|
ENST00000360480.7:c.1647C>T
|
ENSP00000353668.3:p.Asp549=
|
|
ENST00000370224.5:c.1647C>T
|
ENSP00000359244.2:p.Asp549=
|
|
ENST00000625514.2:c.1611C>T
|
ENSP00000486040.1:p.Asp537=
|
|
ENST00000626839.2:c.1677C>T
|
ENSP00000486706.1:p.Asp559=
|
|
ENST00000629241.2:c.1647C>T
|
ENSP00000487142.1:p.Asp549=
|
|
ENST00000629318.1:c.339C>T
|
ENSP00000487384.1:p.Asp113=
|
|
ENST00000629676.2:c.1647C>T
|
ENSP00000486194.1:p.Asp549=
|
|
NM_004518.4:c.1647C>T
|
NP_004509.2:p.Asp549=
|
|
NM_172106.1:c.1677C>T
|
NP_742104.1:p.Asp559=
|
|
NM_172107.2:c.1731C>T
|
NP_742105.1:p.Asp577=
|
|
NM_172108.3:c.1638C>T
|
NP_742106.1:p.Asp546=
|
|
XM_006723787.1:c.1731C>T
|
XP_006723850.1:p.Asp577=
|
|
XM_011528807.1:c.1731C>T
|
XP_011527109.1:p.Asp577=
|
|
XM_011528808.1:c.1728C>T
|
XP_011527110.1:p.Asp576=
|
|
XM_011528809.1:c.1701C>T
|
XP_011527111.1:p.Asp567=
|
|
XM_011528810.1:c.1677C>T
|
XP_011527112.1:p.Asp559=
|
|
XM_011528811.1:c.1647C>T
|
XP_011527113.1:p.Asp549=
|
|
XM_011528812.1:c.1728C>T
|
XP_011527114.1:p.Asp576=
|
|
XM_011528813.1:c.1605C>T
|
XP_011527115.1:p.Asp535=
|
|
XM_011528814.1:c.1212C>T
|
XP_011527116.1:p.Asp404=
|
|
XM_011528815.1:c.1731C>T
|
XP_011527117.1:p.Asp577=
|
|
NM_004518.5:c.1647C>T
|
NP_004509.2:p.Asp549=
|
|
NM_172106.2:c.1677C>T
|
NP_742104.1:p.Asp559=
|
|
NM_172107.3:c.1731C>T
|
NP_742105.1:p.Asp577=
|
|
NM_172108.4:c.1638C>T
|
NP_742106.1:p.Asp546=
|
|
XM_011528810.2:c.1677C>T
|
XP_011527112.1:p.Asp559=
|
|
XM_011528811.2:c.1647C>T
|
XP_011527113.1:p.Asp549=
|
|
XM_017027841.2:c.1674C>T
|
XP_016883330.1:p.Asp558=
|
|
XM_017027842.2:c.1677C>T
|
XP_016883331.1:p.Asp559=
|
|
XM_017027843.1:c.1608C>T
|
XP_016883332.1:p.Asp536=
|
|
XM_017027844.2:c.1674C>T
|
XP_016883333.1:p.Asp558=
|
|
XM_017027845.1:c.639C>T
|
XP_016883334.1:p.Asp213=
|
|
NM_004518.6:c.1647C>T
|
NP_004509.2:p.Asp549=
|
|
NM_172106.3:c.1677C>T
|
NP_742104.1:p.Asp559=
|
|
NM_172107.4:c.1731C>T
MANE Select
|
NP_742105.1:p.Asp577=
|
|
NM_172108.5:c.1638C>T
|
NP_742106.1:p.Asp546=
|
|
NM_001382235.1:c.1677C>T
|
NP_001369164.1:p.Asp559=
|
|