ENST00000221486.6:c.111C>G
(RNASEH2A)
MANE Select
|
ENSP00000221486.4:p.Gly37=
|
|
ENST00000590121.2:c.108C>G
(RNASEH2A)
|
ENSP00000495087.1:p.Gly36=
|
|
ENST00000590279.2:n.193C>G
(RNASEH2A)
|
|
|
ENST00000593017.2:n.101C>G
(RNASEH2A)
|
|
|
ENST00000639767.2:c.*7-224C>G
(THSD8)
|
ENSP00000491410.2:n.*7-224C>G
|
|
ENST00000643364.1:n.795C>G
(THSD8)
|
|
|
ENST00000646769.1:c.111C>G
(RNASEH2A)
|
ENSP00000495175.1:p.Gly37=
|
|
ENST00000221486.4:c.111C>G
(RNASEH2A)
|
ENSP00000221486.3:p.Gly37=
|
|
ENST00000589765.1:n.41+18394G>C
(HOOK2)
|
|
|
ENST00000590121.1:n.108C>G
(RNASEH2A)
|
|
|
ENST00000590279.1:n.101C>G
(RNASEH2A)
|
|
|
ENST00000593017.1:n.193C>G
(RNASEH2A)
|
|
|
NM_006397.2:c.111C>G , LRG_278t1:c.111C>G
(RNASEH2A)
|
NP_006388.2:p.Gly37=
|
|
XM_006722619.2:c.-5-224C>G
(RNASEH2A)
|
XP_006722682.1:n.-5-224C>G
|
|
NM_006397.3:c.111C>G
(RNASEH2A)
MANE Select
|
NP_006388.2:p.Gly37=
|
|