ENST00000289473.11:c.1068G>A
MANE Select
|
ENSP00000289473.4:p.Thr356=
|
|
ENST00000289473.10:c.1068G>A
|
ENSP00000289473.4:p.Thr356=
|
|
ENST00000289473.8:c.1068G>A
|
ENSP00000289473.4:p.Thr356=
|
|
ENST00000398421.6:n.2095G>A
|
|
|
ENST00000455062.2:n.1177G>A
|
|
|
NM_000265.5:c.1068G>A
|
NP_000256.4:p.Thr356=
|
|
XM_005250543.3:c.1030G>A
|
XP_005250600.2:p.Ala344Thr
|
|
XM_011516498.1:c.1067G>A
|
XP_011514800.1:p.Arg356His
|
|
XM_011516501.1:c.675G>A
|
XP_011514803.1:p.Thr225=
|
|
NM_000265.6:c.1068G>A
|
NP_000256.4:p.Thr356=
|
|
NM_000265.7:c.1068G>A
MANE Select
|
NP_000256.4:p.Thr356=
|
|