ENST00000326003.7:c.725T>G
MANE Select
|
ENSP00000314151.1:p.Leu242Arg
|
|
ENST00000326003.6:c.725T>G
|
ENSP00000314151.1:p.Leu242Arg
|
|
ENST00000360617.7:c.1167T>G
|
ENSP00000353829.2:n.1167T>G
|
|
ENST00000422986.6:c.*381T>G
|
ENSP00000393628.2:n.*381T>G
|
|
ENST00000595392.5:c.*226T>G
|
ENSP00000468912.1:n.*226T>G
|
|
ENST00000595952.5:c.596T>G
|
ENSP00000471155.1:p.Leu199Arg
|
|
ENST00000596333.1:n.903T>G
|
|
|
ENST00000598145.1:c.727T>G
|
|
|
ENST00000601349.5:n.2004T>G
|
|
|
ENST00000601812.1:n.1157T>G
|
|
|
ENST00000617027.4:c.602T>G
|
ENSP00000483513.1:p.Leu201Arg
|
|
NM_001030047.1:c.*450T>G
|
NP_001025218.1:n.*450T>G
|
|
NM_001030048.1:c.596T>G
|
NP_001025219.1:p.Leu199Arg
|
|
NM_001648.2:c.725T>G
MANE Select
|
NP_001639.1:p.Leu242Arg
|
|
XM_011526923.1:c.743T>G
|
XP_011525225.1:p.Leu248Arg
|
|
XR_935817.1:n.1324+812T>G
|
|
|