ENST00000329066.9:c.2035A>T
MANE Select
|
ENSP00000329869.4:p.Thr679Ser
|
|
ENST00000329066.8:c.2035A>T
|
ENSP00000329869.4:p.Thr679Ser
|
|
ENST00000345913.8:c.2035A>T
|
ENSP00000318820.7:p.Thr679Ser
|
|
ENST00000346956.7:c.2035A>T
|
ENSP00000263886.6:p.Thr679Ser
|
|
ENST00000382198.5:c.1516A>T
|
ENSP00000371633.1:p.Thr506Ser
|
|
ENST00000382201.7:c.1864A>T
|
ENSP00000371636.3:p.Thr622Ser
|
|
ENST00000422464.5:c.1822A>T
|
ENSP00000405788.1:p.Thr608Ser
|
|
ENST00000446278.5:c.459A>T
|
|
|
ENST00000462973.5:n.424+1978A>T
|
|
|
ENST00000469607.3:c.457A>T
|
ENSP00000419461.1:p.Thr153Ser
|
|
ENST00000497517.6:n.677+1978A>T
|
|
|
NM_000547.5:c.2035A>T
|
NP_000538.3:p.Thr679Ser
|
|
NM_001206744.1:c.2035A>T
|
NP_001193673.1:p.Thr679Ser
|
|
NM_001206745.1:c.1864A>T
|
NP_001193674.1:p.Thr622Ser
|
|
NM_175719.3:c.1864A>T
|
NP_783650.1:p.Thr622Ser
|
|
NM_175721.3:c.2035A>T
|
NP_783652.1:p.Thr679Ser
|
|
NM_175722.3:c.1516A>T
|
NP_783653.1:p.Thr506Ser
|
|
XM_011510379.1:c.2035A>T
|
XP_011508681.1:p.Thr679Ser
|
|
XM_011510380.1:c.2035A>T
|
XP_011508682.1:p.Thr679Ser
|
|
XM_011510381.1:c.1864A>T
|
XP_011508683.1:p.Thr622Ser
|
|
XR_922681.1:n.2036A>T
|
|
|
XM_011510380.3:c.2071A>T
|
XP_011508682.2:p.Thr691Ser
|
|
XM_024453085.1:c.2071A>T
|
XP_024308853.1:p.Thr691Ser
|
|
XM_024453086.1:c.2071A>T
|
XP_024308854.1:p.Thr691Ser
|
|
XM_024453087.1:c.2035A>T
|
XP_024308855.1:p.Thr679Ser
|
|
XM_024453088.1:c.2035A>T
|
XP_024308856.1:p.Thr679Ser
|
|
XM_024453089.1:c.2035A>T
|
XP_024308857.1:p.Thr679Ser
|
|
XM_024453090.1:c.2071A>T
|
XP_024308858.1:p.Thr691Ser
|
|
XM_024453091.1:c.1900A>T
|
XP_024308859.1:p.Thr634Ser
|
|
XM_024453092.1:c.1900A>T
|
XP_024308860.1:p.Thr634Ser
|
|
XM_024453093.1:c.1552A>T
|
XP_024308861.1:p.Thr518Ser
|
|
NM_001206744.2:c.2035A>T
MANE Select
|
NP_001193673.1:p.Thr679Ser
|
|
NM_000547.6:c.2035A>T
|
NP_000538.3:p.Thr679Ser
|
|
NM_001206745.2:c.1864A>T
|
NP_001193674.1:p.Thr622Ser
|
|
NM_175719.4:c.1864A>T
|
NP_783650.1:p.Thr622Ser
|
|