ENST00000706989.1:c.2036C>T
|
ENSP00000516702.1:p.Ala679Val
|
|
ENST00000359125.7:c.1982C>T
MANE Select
|
ENSP00000352035.2:p.Ala661Val
|
|
ENST00000637193.1:c.1379C>T
|
ENSP00000490734.1:p.Ala460Val
|
|
ENST00000344462.8:c.1889C>T
|
ENSP00000339611.4:p.Ala630Val
|
|
ENST00000357249.6:c.1550C>T
|
ENSP00000349789.3:p.Ala517Val
|
|
ENST00000359125.6:c.1982C>T
|
ENSP00000352035.2:p.Ala661Val
|
|
ENST00000360480.7:c.1898C>T
|
ENSP00000353668.3:p.Ala633Val
|
|
ENST00000370224.5:c.2006C>T
|
ENSP00000359244.2:p.Ala669Val
|
|
ENST00000625514.2:c.1970C>T
|
ENSP00000486040.1:p.Ala657Val
|
|
ENST00000626839.2:c.1928C>T
|
ENSP00000486706.1:p.Ala643Val
|
|
ENST00000629241.2:c.1898C>T
|
ENSP00000487142.1:p.Ala633Val
|
|
ENST00000629676.2:c.1679+6169C>T
|
ENSP00000486194.1:n.1679+6169C>T
|
|
NM_004518.4:c.1898C>T
|
NP_004509.2:p.Ala633Val
|
|
NM_172106.1:c.1928C>T
|
NP_742104.1:p.Ala643Val
|
|
NM_172107.2:c.1982C>T
|
NP_742105.1:p.Ala661Val
|
|
NM_172108.3:c.1889C>T
|
NP_742106.1:p.Ala630Val
|
|
XM_006723787.1:c.2024C>T
|
XP_006723850.1:p.Ala675Val
|
|
XM_011528807.1:c.2090C>T
|
XP_011527109.1:p.Ala697Val
|
|
XM_011528808.1:c.2087C>T
|
XP_011527110.1:p.Ala696Val
|
|
XM_011528809.1:c.2060C>T
|
XP_011527111.1:p.Ala687Val
|
|
XM_011528810.1:c.2036C>T
|
XP_011527112.1:p.Ala679Val
|
|
XM_011528811.1:c.2006C>T
|
XP_011527113.1:p.Ala669Val
|
|
XM_011528812.1:c.1979C>T
|
XP_011527114.1:p.Ala660Val
|
|
XM_011528813.1:c.1964C>T
|
XP_011527115.1:p.Ala655Val
|
|
XM_011528814.1:c.1571C>T
|
XP_011527116.1:p.Ala524Val
|
|
NM_004518.5:c.1898C>T
|
NP_004509.2:p.Ala633Val
|
|
NM_172106.2:c.1928C>T
|
NP_742104.1:p.Ala643Val
|
|
NM_172107.3:c.1982C>T
|
NP_742105.1:p.Ala661Val
|
|
NM_172108.4:c.1889C>T
|
NP_742106.1:p.Ala630Val
|
|
XM_011528810.2:c.2036C>T
|
XP_011527112.1:p.Ala679Val
|
|
XM_011528811.2:c.2006C>T
|
XP_011527113.1:p.Ala669Val
|
|
XM_017027841.2:c.2033C>T
|
XP_016883330.1:p.Ala678Val
|
|
XM_017027842.2:c.1970C>T
|
XP_016883331.1:p.Ala657Val
|
|
XM_017027843.1:c.1967C>T
|
XP_016883332.1:p.Ala656Val
|
|
XM_017027844.2:c.1925C>T
|
XP_016883333.1:p.Ala642Val
|
|
XM_017027845.1:c.998C>T
|
XP_016883334.1:p.Ala333Val
|
|
NM_004518.6:c.1898C>T
|
NP_004509.2:p.Ala633Val
|
|
NM_172106.3:c.1928C>T
|
NP_742104.1:p.Ala643Val
|
|
NM_172107.4:c.1982C>T
MANE Select
|
NP_742105.1:p.Ala661Val
|
|
NM_172108.5:c.1889C>T
|
NP_742106.1:p.Ala630Val
|
|
NM_001382235.1:c.2036C>T
|
NP_001369164.1:p.Ala679Val
|
|