ENST00000295897.9:c.715G=
MANE Select
|
ENSP00000295897.4:p.Ala239=
|
|
ENST00000295897.8:c.715G=
|
ENSP00000295897.4:p.Ala239=
|
|
ENST00000401494.7:c.370G=
|
ENSP00000384695.3:p.Ala124=
|
|
ENST00000415165.6:c.139G=
|
ENSP00000401820.2:p.Ala47=
|
|
ENST00000476441.6:c.312G=
|
ENSP00000423727.1:p.Gly104=
|
|
ENST00000503124.5:c.265G=
|
ENSP00000421027.1:p.Ala89=
|
|
ENST00000505649.5:n.401G=
|
|
|
ENST00000507673.1:n.32G=
|
|
|
ENST00000509063.5:c.715G=
|
ENSP00000422784.1:p.Ala239=
|
|
ENST00000511370.1:c.248G=
|
|
|
ENST00000621085.4:c.490+2635G=
|
ENSP00000483421.1:n.490+2635G=
|
|
ENST00000621628.4:c.486+2921G=
|
ENSP00000480485.1:n.486+2921G=
|
|
NM_000477.5:c.715G=
|
NP_000468.1:p.Ala239=
|
|
NM_000477.6:c.715G=
|
NP_000468.1:p.Ala239=
|
|
NM_000477.7:c.715G=
MANE Select
|
NP_000468.1:p.Ala239=
|
|