ENST00000221431.11:c.17C>G
(SARS2)
MANE Select
|
ENSP00000221431.6:p.Ala6Gly
|
|
ENST00000221431.10:c.17C>G
(SARS2)
|
ENSP00000221431.5:p.Ala6Gly
|
|
ENST00000308018.8:c.-298G>C
(MRPS12)
|
ENSP00000308845.3:n.-298G>C
|
|
ENST00000430193.7:c.17C>G
(SARS2)
|
ENSP00000406754.3:p.Ala6Gly
|
|
ENST00000455102.6:c.17C>G
(SARS2)
|
ENSP00000414954.2:p.Ala6Gly
|
|
ENST00000593754.1:c.17C>G
(SARS2)
|
ENSP00000471767.1:p.Ala6Gly
|
|
ENST00000598343.5:c.17C>G
(SARS2)
|
ENSP00000472576.1:p.Ala6Gly
|
|
ENST00000598598.5:n.44C>G
(SARS2)
|
|
|
ENST00000599996.1:c.476-4420C>G
|
|
|
ENST00000600042.5:c.17C>G
(SARS2)
|
ENSP00000472847.1:p.Ala6Gly
|
|
NM_001145901.1:c.17C>G
(SARS2)
|
NP_001139373.1:p.Ala6Gly
|
|
NM_017827.3:c.17C>G
(SARS2)
|
NP_060297.1:p.Ala6Gly
|
|
NM_033362.3:c.-298G>C
(MRPS12)
|
NP_203526.1:n.-298G>C
|
|
NM_001145901.2:c.17C>G
(SARS2)
|
NP_001139373.1:p.Ala6Gly
|
|
NM_017827.4:c.17C>G
(SARS2)
MANE Select
|
NP_060297.1:p.Ala6Gly
|
|