ENST00000378585.7:c.122T>G
MANE Select
|
ENSP00000367848.4:p.Leu41Arg
|
|
ENST00000638411.1:c.122T>G
|
ENSP00000491632.1:p.Leu41Arg
|
|
ENST00000638604.1:n.186T>G
|
|
|
ENST00000638771.1:c.122T>G
|
ENSP00000492435.1:p.Leu41Arg
|
|
ENST00000639045.1:c.*108T>G
|
ENSP00000491997.1:n.*108T>G
|
|
ENST00000639777.1:n.726T>G
|
|
|
ENST00000639935.1:n.159T>G
|
|
|
ENST00000640030.1:c.62T>G
|
ENSP00000491411.1:p.Leu21Arg
|
|
ENST00000640067.1:c.122T>G
|
ENSP00000491844.1:p.Leu41Arg
|
|
ENST00000640423.1:n.131T>G
|
|
|
ENST00000640949.1:c.122T>G
|
ENSP00000492500.1:p.Leu41Arg
|
|
ENST00000378585.5:c.122T>G
|
ENSP00000367848.4:p.Leu41Arg
|
|
NM_000815.4:c.122T>G
|
NP_000806.2:p.Leu41Arg
|
|
XM_011541194.1:c.161T>G
|
XP_011539496.1:p.Leu54Arg
|
|
XM_011541194.3:c.161T>G
|
XP_011539496.1:p.Leu54Arg
|
|
XM_017000936.1:c.827T>G
|
XP_016856425.1:p.Leu276Arg
|
|
NM_000815.5:c.122T>G
MANE Select
|
NP_000806.2:p.Leu41Arg
|
|