|
ENST00000219833.13:c.1164C>G
|
ENSP00000219833.8:p.Phe388Leu
|
|
|
ENST00000568943.6:c.1164C>G
MANE Select
|
ENSP00000457473.1:p.Phe388Leu
|
|
|
ENST00000574918.2:c.1029C>G
|
ENSP00000460214.2:p.Phe343Leu
|
|
|
ENST00000682050.1:c.1012+839C>G
|
ENSP00000508367.1:n.1012+839C>G
|
|
|
ENST00000219833.12:c.1164C>G
|
ENSP00000219833.8:p.Phe388Leu
|
|
|
ENST00000379906.6:c.1164C>G
|
ENSP00000369237.2:p.Phe388Leu
|
|
|
ENST00000414754.7:c.1164C>G
|
ENSP00000394956.3:p.Phe388Leu
|
|
|
ENST00000561820.5:c.1164C>G
|
ENSP00000454439.1:p.Phe388Leu
|
|
|
ENST00000566163.5:c.1029C>G
|
ENSP00000456210.1:p.Phe343Leu
|
|
|
ENST00000567238.1:c.849C>G
|
ENSP00000457375.1:p.Phe283Leu
|
|
|
ENST00000568943.5:c.1164C>G
|
ENSP00000457473.1:p.Phe388Leu
|
|
|
NM_001043.3:c.1164C>G
|
NP_001034.1:p.Phe388Leu
|
|
|
NM_001172501.1:c.1164C>G
|
NP_001165972.1:p.Phe388Leu
|
|
|
NM_001172502.1:c.849C>G
|
NP_001165973.1:p.Phe283Leu
|
|
|
NM_001172504.1:c.1164C>G
|
NP_001165975.1:p.Phe388Leu
|
|
|
XM_006721263.2:c.1164C>G
|
XP_006721326.1:p.Phe388Leu
|
|
|
XM_011523295.1:c.1164C>G
|
XP_011521597.1:p.Phe388Leu
|
|
|
XM_011523296.1:c.1029C>G
|
XP_011521598.1:p.Phe343Leu
|
|
|
XM_011523297.1:c.1029C>G
|
XP_011521599.1:p.Phe343Leu
|
|
|
XM_011523298.1:c.1147+839C>G
|
XP_011521600.1:n.1147+839C>G
|
|
|
XM_011523299.1:c.441C>G
|
XP_011521601.1:p.Phe147Leu
|
|
|
XM_011523300.1:c.441C>G
|
XP_011521602.1:p.Phe147Leu
|
|
|
XR_933403.1:n.1781C>G
|
|
|
|
XM_011523295.2:c.1164C>G
|
XP_011521597.1:p.Phe388Leu
|
|
|
XM_011523296.2:c.1029C>G
|
XP_011521598.1:p.Phe343Leu
|
|
|
XM_011523297.3:c.1029C>G
|
XP_011521599.1:p.Phe343Leu
|
|
|
XM_011523298.2:c.1147+839C>G
|
XP_011521600.1:n.1147+839C>G
|
|
|
XM_011523299.2:c.441C>G
|
XP_011521601.1:p.Phe147Leu
|
|
|
XM_011523300.2:c.441C>G
|
XP_011521602.1:p.Phe147Leu
|
|
|
XR_933403.3:n.1457C>G
|
|
|
|
NM_001172501.2:c.1164C>G
|
NP_001165972.1:p.Phe388Leu
|
|
|
NM_001172501.3:c.1164C>G
MANE Select
|
NP_001165972.1:p.Phe388Leu
|
|
