ENST00000295897.9:c.1142T>G
MANE Select
|
ENSP00000295897.4:p.Leu381Arg
|
|
ENST00000295897.8:c.1142T>G
|
ENSP00000295897.4:p.Leu381Arg
|
|
ENST00000401494.7:c.797T>G
|
ENSP00000384695.3:p.Leu266Arg
|
|
ENST00000415165.6:c.566T>G
|
ENSP00000401820.2:p.Leu189Arg
|
|
ENST00000476441.6:c.*421T>G
|
ENSP00000423727.1:n.*421T>G
|
|
ENST00000484992.1:n.462T>G
|
|
|
ENST00000503124.5:c.692T>G
|
ENSP00000421027.1:p.Leu231Arg
|
|
ENST00000504043.1:n.145T>G
|
|
|
ENST00000505649.5:n.828T>G
|
|
|
ENST00000509063.5:c.1142T>G
|
ENSP00000422784.1:p.Leu381Arg
|
|
ENST00000511370.1:c.675T>G
|
|
|
ENST00000621085.4:c.503T>G
|
ENSP00000483421.1:p.Leu168Arg
|
|
ENST00000621628.4:c.503T>G
|
ENSP00000480485.1:p.Leu168Arg
|
|
NM_000477.5:c.1142T>G
|
NP_000468.1:p.Leu381Arg
|
|
NM_000477.6:c.1142T>G
|
NP_000468.1:p.Leu381Arg
|
|
NM_000477.7:c.1142T>G
MANE Select
|
NP_000468.1:p.Leu381Arg
|
|