ENST00000394867.9:n.1605T>G
|
|
|
ENST00000688002.1:n.3317T>G
|
|
|
ENST00000688751.1:n.302T>G
|
|
|
ENST00000689792.1:n.1070T>G
|
|
|
ENST00000262948.10:c.1166T>G
MANE Select
|
ENSP00000262948.4:p.Leu389Arg
|
|
ENST00000262948.9:c.1166T>G
|
ENSP00000262948.3:p.Leu389Arg
|
|
ENST00000394867.8:c.875T>G
|
ENSP00000378336.1:p.Leu292Arg
|
|
ENST00000597263.5:n.351T>G
|
|
|
ENST00000599021.1:c.276T>G
|
|
|
ENST00000600584.5:n.2615T>G
|
|
|
ENST00000601786.5:n.1467T>G
|
|
|
NM_030662.3:c.1166T>G , LRG_750t1:c.1166T>G
|
NP_109587.1:p.Leu389Arg
|
|
XM_006722799.2:c.887T>G
|
XP_006722862.1:p.Leu296Arg
|
|
XM_011528133.1:c.596T>G
|
XP_011526435.1:p.Leu199Arg
|
|
NM_030662.4:c.1166T>G
MANE Select
|
NP_109587.1:p.Leu389Arg
|
|