|
ENST00000329066.9:c.1037C>G
MANE Select
|
ENSP00000329869.4:p.Ala346Gly
|
|
|
ENST00000329066.8:c.1037C>G
|
ENSP00000329869.4:p.Ala346Gly
|
|
|
ENST00000345913.8:c.1037C>G
|
ENSP00000318820.7:p.Ala346Gly
|
|
|
ENST00000346956.7:c.1037C>G
|
ENSP00000263886.6:p.Ala346Gly
|
|
|
ENST00000382198.5:c.820-7293C>G
|
ENSP00000371633.1:n.820-7293C>G
|
|
|
ENST00000382201.7:c.1037C>G
|
ENSP00000371636.3:p.Ala346Gly
|
|
|
ENST00000422464.5:c.824C>G
|
ENSP00000405788.1:p.Ala275Gly
|
|
|
ENST00000497517.6:n.181-7293C>G
|
|
|
|
NM_000547.5:c.1037C>G
|
NP_000538.3:p.Ala346Gly
|
|
|
NM_001206744.1:c.1037C>G
|
NP_001193673.1:p.Ala346Gly
|
|
|
NM_001206745.1:c.1037C>G
|
NP_001193674.1:p.Ala346Gly
|
|
|
NM_175719.3:c.1037C>G
|
NP_783650.1:p.Ala346Gly
|
|
|
NM_175721.3:c.1037C>G
|
NP_783652.1:p.Ala346Gly
|
|
|
NM_175722.3:c.820-7293C>G
|
NP_783653.1:n.820-7293C>G
|
|
|
XM_011510379.1:c.1037C>G
|
XP_011508681.1:p.Ala346Gly
|
|
|
XM_011510380.1:c.1037C>G
|
XP_011508682.1:p.Ala346Gly
|
|
|
XM_011510381.1:c.1037C>G
|
XP_011508683.1:p.Ala346Gly
|
|
|
XM_011510382.1:c.1037C>G
|
XP_011508684.1:p.Ala346Gly
|
|
|
XR_922681.1:n.1038C>G
|
|
|
|
XM_011510380.3:c.1073C>G
|
XP_011508682.2:p.Ala358Gly
|
|
|
XM_024453085.1:c.1073C>G
|
XP_024308853.1:p.Ala358Gly
|
|
|
XM_024453086.1:c.1073C>G
|
XP_024308854.1:p.Ala358Gly
|
|
|
XM_024453087.1:c.1037C>G
|
XP_024308855.1:p.Ala346Gly
|
|
|
XM_024453088.1:c.1037C>G
|
XP_024308856.1:p.Ala346Gly
|
|
|
XM_024453089.1:c.1037C>G
|
XP_024308857.1:p.Ala346Gly
|
|
|
XM_024453090.1:c.1073C>G
|
XP_024308858.1:p.Ala358Gly
|
|
|
XM_024453091.1:c.1073C>G
|
XP_024308859.1:p.Ala358Gly
|
|
|
XM_024453092.1:c.1073C>G
|
XP_024308860.1:p.Ala358Gly
|
|
|
XM_024453093.1:c.856-7293C>G
|
XP_024308861.1:n.856-7293C>G
|
|
|
NM_001206744.2:c.1037C>G
MANE Select
|
NP_001193673.1:p.Ala346Gly
|
|
|
NM_000547.6:c.1037C>G
|
NP_000538.3:p.Ala346Gly
|
|
|
NM_001206745.2:c.1037C>G
|
NP_001193674.1:p.Ala346Gly
|
|
|
NM_175719.4:c.1037C>G
|
NP_783650.1:p.Ala346Gly
|
|
