ENST00000706989.1:c.1946T>G
|
ENSP00000516702.1:p.Leu649Trp
|
|
ENST00000359125.7:c.1892T>G
MANE Select
|
ENSP00000352035.2:p.Leu631Trp
|
|
ENST00000637193.1:c.1289T>G
|
ENSP00000490734.1:p.Leu430Trp
|
|
ENST00000637338.1:n.49T>G
|
|
|
ENST00000344462.8:c.1799T>G
|
ENSP00000339611.4:p.Leu600Trp
|
|
ENST00000357249.6:c.1460T>G
|
ENSP00000349789.3:p.Leu487Trp
|
|
ENST00000359125.6:c.1892T>G
|
ENSP00000352035.2:p.Leu631Trp
|
|
ENST00000360480.7:c.1808T>G
|
ENSP00000353668.3:p.Leu603Trp
|
|
ENST00000370224.5:c.1916T>G
|
ENSP00000359244.2:p.Leu639Trp
|
|
ENST00000625514.2:c.1880T>G
|
ENSP00000486040.1:p.Leu627Trp
|
|
ENST00000626839.2:c.1838T>G
|
ENSP00000486706.1:p.Leu613Trp
|
|
ENST00000629241.2:c.1808T>G
|
ENSP00000487142.1:p.Leu603Trp
|
|
ENST00000629676.2:c.1679+6079T>G
|
ENSP00000486194.1:n.1679+6079T>G
|
|
NM_004518.4:c.1808T>G
|
NP_004509.2:p.Leu603Trp
|
|
NM_172106.1:c.1838T>G
|
NP_742104.1:p.Leu613Trp
|
|
NM_172107.2:c.1892T>G
|
NP_742105.1:p.Leu631Trp
|
|
NM_172108.3:c.1799T>G
|
NP_742106.1:p.Leu600Trp
|
|
XM_006723787.1:c.1934T>G
|
XP_006723850.1:p.Leu645Trp
|
|
XM_011528807.1:c.2000T>G
|
XP_011527109.1:p.Leu667Trp
|
|
XM_011528808.1:c.1997T>G
|
XP_011527110.1:p.Leu666Trp
|
|
XM_011528809.1:c.1970T>G
|
XP_011527111.1:p.Leu657Trp
|
|
XM_011528810.1:c.1946T>G
|
XP_011527112.1:p.Leu649Trp
|
|
XM_011528811.1:c.1916T>G
|
XP_011527113.1:p.Leu639Trp
|
|
XM_011528812.1:c.1889T>G
|
XP_011527114.1:p.Leu630Trp
|
|
XM_011528813.1:c.1874T>G
|
XP_011527115.1:p.Leu625Trp
|
|
XM_011528814.1:c.1481T>G
|
XP_011527116.1:p.Leu494Trp
|
|
NM_004518.5:c.1808T>G
|
NP_004509.2:p.Leu603Trp
|
|
NM_172106.2:c.1838T>G
|
NP_742104.1:p.Leu613Trp
|
|
NM_172107.3:c.1892T>G
|
NP_742105.1:p.Leu631Trp
|
|
NM_172108.4:c.1799T>G
|
NP_742106.1:p.Leu600Trp
|
|
XM_011528810.2:c.1946T>G
|
XP_011527112.1:p.Leu649Trp
|
|
XM_011528811.2:c.1916T>G
|
XP_011527113.1:p.Leu639Trp
|
|
XM_017027841.2:c.1943T>G
|
XP_016883330.1:p.Leu648Trp
|
|
XM_017027842.2:c.1880T>G
|
XP_016883331.1:p.Leu627Trp
|
|
XM_017027843.1:c.1877T>G
|
XP_016883332.1:p.Leu626Trp
|
|
XM_017027844.2:c.1835T>G
|
XP_016883333.1:p.Leu612Trp
|
|
XM_017027845.1:c.908T>G
|
XP_016883334.1:p.Leu303Trp
|
|
NM_004518.6:c.1808T>G
|
NP_004509.2:p.Leu603Trp
|
|
NM_172106.3:c.1838T>G
|
NP_742104.1:p.Leu613Trp
|
|
NM_172107.4:c.1892T>G
MANE Select
|
NP_742105.1:p.Leu631Trp
|
|
NM_172108.5:c.1799T>G
|
NP_742106.1:p.Leu600Trp
|
|
NM_001382235.1:c.1946T>G
|
NP_001369164.1:p.Leu649Trp
|
|