ENST00000326003.7:c.707T>G
MANE Select
|
ENSP00000314151.1:p.Leu236Arg
|
|
ENST00000326003.6:c.707T>G
|
ENSP00000314151.1:p.Leu236Arg
|
|
ENST00000360617.7:c.1149T>G
|
ENSP00000353829.2:n.1149T>G
|
|
ENST00000422986.6:c.*363T>G
|
ENSP00000393628.2:n.*363T>G
|
|
ENST00000595392.5:c.*208T>G
|
ENSP00000468912.1:n.*208T>G
|
|
ENST00000595952.5:c.578T>G
|
ENSP00000471155.1:p.Leu193Arg
|
|
ENST00000596333.1:n.885T>G
|
|
|
ENST00000598145.1:c.709T>G
|
|
|
ENST00000601349.5:n.1986T>G
|
|
|
ENST00000601812.1:n.1139T>G
|
|
|
ENST00000617027.4:c.584T>G
|
ENSP00000483513.1:p.Leu195Arg
|
|
NM_001030047.1:c.*432T>G
|
NP_001025218.1:n.*432T>G
|
|
NM_001030048.1:c.578T>G
|
NP_001025219.1:p.Leu193Arg
|
|
NM_001648.2:c.707T>G
MANE Select
|
NP_001639.1:p.Leu236Arg
|
|
XM_011526923.1:c.725T>G
|
XP_011525225.1:p.Leu242Arg
|
|
XR_935817.1:n.1324+794T>G
|
|
|