ENST00000295897.9:c.589G=
MANE Select
|
ENSP00000295897.4:p.Asp197=
|
|
ENST00000295897.8:c.589G=
|
ENSP00000295897.4:p.Asp197=
|
|
ENST00000401494.7:c.244G=
|
ENSP00000384695.3:p.Asp82=
|
|
ENST00000415165.6:c.138-2535G=
|
ENSP00000401820.2:n.138-2535G=
|
|
ENST00000476441.6:c.186G=
|
ENSP00000423727.1:p.Leu62=
|
|
ENST00000503124.5:c.139G=
|
ENSP00000421027.1:p.Asp47=
|
|
ENST00000505649.5:n.275G=
|
|
|
ENST00000509063.5:c.589G=
|
ENSP00000422784.1:p.Asp197=
|
|
ENST00000511370.1:c.122G=
|
|
|
ENST00000514786.1:n.558G=
|
|
|
ENST00000621085.4:c.490+99G=
|
ENSP00000483421.1:n.490+99G=
|
|
ENST00000621628.4:c.486+385G=
|
ENSP00000480485.1:n.486+385G=
|
|
NM_000477.5:c.589G=
|
NP_000468.1:p.Asp197=
|
|
NM_000477.6:c.589G=
|
NP_000468.1:p.Asp197=
|
|
NM_000477.7:c.589G=
MANE Select
|
NP_000468.1:p.Asp197=
|
|