ENST00000295897.9:c.1822G>C
MANE Select
|
ENSP00000295897.4:p.Gly608Arg
|
|
ENST00000295897.8:c.1822G>C
|
ENSP00000295897.4:p.Gly608Arg
|
|
ENST00000401494.7:c.1477G>C
|
ENSP00000384695.3:p.Gly493Arg
|
|
ENST00000415165.6:c.1246G>C
|
ENSP00000401820.2:p.Gly416Arg
|
|
ENST00000476441.6:c.*1101G>C
|
ENSP00000423727.1:n.*1101G>C
|
|
ENST00000495173.1:n.130G>C
|
|
|
ENST00000503124.5:c.1372G>C
|
ENSP00000421027.1:p.Gly458Arg
|
|
ENST00000505649.5:n.1369G>C
|
|
|
ENST00000508932.5:n.212G>C
|
|
|
ENST00000509063.5:c.1785+651G>C
|
ENSP00000422784.1:n.1785+651G>C
|
|
ENST00000511370.1:c.1355G>C
|
|
|
ENST00000621085.4:c.1183G>C
|
ENSP00000483421.1:p.Gly395Arg
|
|
ENST00000621628.4:c.1183G>C
|
ENSP00000480485.1:p.Gly395Arg
|
|
NM_000477.5:c.1822G>C
|
NP_000468.1:p.Gly608Arg
|
|
NM_000477.6:c.1822G>C
|
NP_000468.1:p.Gly608Arg
|
|
NM_000477.7:c.1822G>C
MANE Select
|
NP_000468.1:p.Gly608Arg
|
|