ENST00000295897.9:c.569C>G
MANE Select
|
ENSP00000295897.4:p.Thr190Arg
|
|
ENST00000295897.8:c.569C>G
|
ENSP00000295897.4:p.Thr190Arg
|
|
ENST00000401494.7:c.224C>G
|
ENSP00000384695.3:p.Thr75Arg
|
|
ENST00000415165.6:c.138-2555C>G
|
ENSP00000401820.2:n.138-2555C>G
|
|
ENST00000441319.5:c.575C>G
|
ENSP00000392541.1:p.Thr192Arg
|
|
ENST00000476441.6:c.166C>G
|
ENSP00000423727.1:p.Gln56Glu
|
|
ENST00000503124.5:c.119C>G
|
ENSP00000421027.1:p.Thr40Arg
|
|
ENST00000505649.5:n.255C>G
|
|
|
ENST00000509063.5:c.569C>G
|
ENSP00000422784.1:p.Thr190Arg
|
|
ENST00000511370.1:c.102C>G
|
|
|
ENST00000514786.1:n.538C>G
|
|
|
ENST00000621085.4:c.490+79C>G
|
ENSP00000483421.1:n.490+79C>G
|
|
ENST00000621628.4:c.486+365C>G
|
ENSP00000480485.1:n.486+365C>G
|
|
NM_000477.5:c.569C>G
|
NP_000468.1:p.Thr190Arg
|
|
NM_000477.6:c.569C>G
|
NP_000468.1:p.Thr190Arg
|
|
NM_000477.7:c.569C>G
MANE Select
|
NP_000468.1:p.Thr190Arg
|
|