ENST00000305264.8:c.967C>G
MANE Select
|
ENSP00000302967.3:p.Leu323Val
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|
ENST00000305264.7:c.967C>G
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ENSP00000302967.3:p.Leu323Val
|
|
ENST00000459727.5:n.233+169C>G
|
|
|
ENST00000467533.5:n.599+169C>G
|
|
|
ENST00000469207.5:n.46C>G
|
|
|
ENST00000469550.6:n.1040C>G
|
|
|
ENST00000486618.1:n.461C>G
|
|
|
ENST00000491581.5:n.181C>G
|
|
|
ENST00000492407.1:n.767+169C>G
|
|
|
NM_003883.3:c.967C>G
|
NP_003874.2:p.Leu323Val
|
|
XM_011537697.1:c.406C>G
|
XP_011535999.1:p.Leu136Val
|
|
XR_944336.1:n.1052C>G
|
|
|
NM_001355039.1:c.967C>G
|
NP_001341968.1:p.Leu323Val
|
|
NM_001355040.1:c.508C>G
|
NP_001341969.1:p.Leu170Val
|
|
NM_001355041.1:c.406C>G
|
NP_001341970.1:p.Leu136Val
|
|
NR_149164.1:n.1033C>G
|
|
|
NR_149165.1:n.915C>G
|
|
|
NR_149166.1:n.843+169C>G
|
|
|
NR_149167.1:n.1011+169C>G
|
|
|
NR_149168.1:n.1058C>G
|
|
|
NR_149169.1:n.1058C>G
|
|
|
NM_003883.4:c.967C>G
MANE Select
|
NP_003874.2:p.Leu323Val
|
|
NM_001355039.2:c.967C>G
|
NP_001341968.1:p.Leu323Val
|
|
NR_149167.2:n.1004+169C>G
|
|
|
NM_001355040.2:c.508C>G
|
NP_001341969.1:p.Leu170Val
|
|
NM_001355041.2:c.406C>G
|
NP_001341970.1:p.Leu136Val
|
|
NR_149164.2:n.1026C>G
|
|
|
NR_149165.2:n.908C>G
|
|
|
NR_149166.2:n.836+169C>G
|
|
|
NR_149168.2:n.1051C>G
|
|
|
NR_149169.2:n.1051C>G
|
|
|