ENST00000295897.9:c.1682C>G
MANE Select
|
ENSP00000295897.4:p.Pro561Arg
|
|
ENST00000295897.8:c.1682C>G
|
ENSP00000295897.4:p.Pro561Arg
|
|
ENST00000401494.7:c.1337C>G
|
ENSP00000384695.3:p.Pro446Arg
|
|
ENST00000415165.6:c.1106C>G
|
ENSP00000401820.2:p.Pro369Arg
|
|
ENST00000476441.6:c.*961C>G
|
ENSP00000423727.1:n.*961C>G
|
|
ENST00000486939.1:n.336C>G
|
|
|
ENST00000503124.5:c.1232C>G
|
ENSP00000421027.1:p.Pro411Arg
|
|
ENST00000505649.5:n.1229C>G
|
|
|
ENST00000508932.5:n.175+81C>G
|
|
|
ENST00000509063.5:c.1682C>G
|
ENSP00000422784.1:p.Pro561Arg
|
|
ENST00000511370.1:c.1215C>G
|
|
|
ENST00000621085.4:c.1043C>G
|
ENSP00000483421.1:p.Pro348Arg
|
|
ENST00000621628.4:c.1043C>G
|
ENSP00000480485.1:p.Pro348Arg
|
|
NM_000477.5:c.1682C>G
|
NP_000468.1:p.Pro561Arg
|
|
NM_000477.6:c.1682C>G
|
NP_000468.1:p.Pro561Arg
|
|
NM_000477.7:c.1682C>G
MANE Select
|
NP_000468.1:p.Pro561Arg
|
|