ENST00000329066.9:c.2416C>G
MANE Select
|
ENSP00000329869.4:p.Pro806Ala
|
|
ENST00000329066.8:c.2416C>G
|
ENSP00000329869.4:p.Pro806Ala
|
|
ENST00000345913.8:c.2416C>G
|
ENSP00000318820.7:p.Pro806Ala
|
|
ENST00000346956.7:c.2386+7212C>G
|
ENSP00000263886.6:n.2386+7212C>G
|
|
ENST00000382198.5:c.1897C>G
|
ENSP00000371633.1:p.Pro633Ala
|
|
ENST00000382201.7:c.2245C>G
|
ENSP00000371636.3:p.Pro749Ala
|
|
ENST00000422464.5:c.2173+7212C>G
|
ENSP00000405788.1:n.2173+7212C>G
|
|
ENST00000425083.3:n.79C>G
|
|
|
ENST00000446278.5:c.840C>G
|
|
|
ENST00000462973.5:n.424+9938C>G
|
|
|
ENST00000469607.3:c.808+7212C>G
|
ENSP00000419461.1:n.808+7212C>G
|
|
ENST00000497517.6:n.707C>G
|
|
|
NM_000547.5:c.2416C>G
|
NP_000538.3:p.Pro806Ala
|
|
NM_001206744.1:c.2416C>G
|
NP_001193673.1:p.Pro806Ala
|
|
NM_001206745.1:c.2245C>G
|
NP_001193674.1:p.Pro749Ala
|
|
NM_175719.3:c.2245C>G
|
NP_783650.1:p.Pro749Ala
|
|
NM_175721.3:c.2386+7212C>G
|
NP_783652.1:n.2386+7212C>G
|
|
NM_175722.3:c.1897C>G
|
NP_783653.1:p.Pro633Ala
|
|
XM_011510379.1:c.2386+7212C>G
|
XP_011508681.1:n.2386+7212C>G
|
|
XM_011510380.1:c.2416C>G
|
XP_011508682.1:p.Pro806Ala
|
|
XM_011510381.1:c.2215+7212C>G
|
XP_011508683.1:n.2215+7212C>G
|
|
XR_922681.1:n.2417C>G
|
|
|
XM_011510380.3:c.2452C>G
|
XP_011508682.2:p.Pro818Ala
|
|
XM_024453085.1:c.2422+7212C>G
|
XP_024308853.1:n.2422+7212C>G
|
|
XM_024453086.1:c.2452C>G
|
XP_024308854.1:p.Pro818Ala
|
|
XM_024453087.1:c.2386+7212C>G
|
XP_024308855.1:n.2386+7212C>G
|
|
XM_024453088.1:c.2386+7212C>G
|
XP_024308856.1:n.2386+7212C>G
|
|
XM_024453089.1:c.2386+7212C>G
|
XP_024308857.1:n.2386+7212C>G
|
|
XM_024453090.1:c.2422+7212C>G
|
XP_024308858.1:n.2422+7212C>G
|
|
XM_024453091.1:c.2281C>G
|
XP_024308859.1:p.Pro761Ala
|
|
XM_024453092.1:c.2251+7212C>G
|
XP_024308860.1:n.2251+7212C>G
|
|
XM_024453093.1:c.1933C>G
|
XP_024308861.1:p.Pro645Ala
|
|
NM_001206744.2:c.2416C>G
MANE Select
|
NP_001193673.1:p.Pro806Ala
|
|
NM_000547.6:c.2416C>G
|
NP_000538.3:p.Pro806Ala
|
|
NM_001206745.2:c.2245C>G
|
NP_001193674.1:p.Pro749Ala
|
|
NM_175719.4:c.2245C>G
|
NP_783650.1:p.Pro749Ala
|
|