|
ENST00000356839.10:c.623-7C>G
MANE Select
|
ENSP00000349297.5:n.623-7C>G
|
|
|
ENST00000322910.9:c.*578-7C>G
|
ENSP00000325395.5:n.*578-7C>G
|
|
|
ENST00000350303.9:c.557-7C>G
|
ENSP00000344152.5:n.557-7C>G
|
|
|
ENST00000356839.9:c.623-7C>G
|
ENSP00000349297.5:n.623-7C>G
|
|
|
ENST00000543245.6:c.692-7C>G
|
ENSP00000438689.2:n.692-7C>G
|
|
|
ENST00000577191.5:n.700-7C>G
|
|
|
|
ENST00000577857.5:n.439-7C>G
|
|
|
|
ENST00000579286.5:n.804-7C>G
|
|
|
|
ENST00000579886.2:c.461-7C>G
|
ENSP00000463246.1:n.461-7C>G
|
|
|
ENST00000580365.1:n.354-7C>G
|
|
|
|
ENST00000581378.5:c.341-7C>G
|
|
|
|
ENST00000581562.5:n.525-7C>G
|
|
|
|
ENST00000583312.5:c.631C>G
|
ENSP00000467920.1:p.Pro211Ala
|
|
|
ENST00000583760.1:n.405-7C>G
|
|
|
|
NM_000018.3:c.623-7C>G
|
NP_000009.1:n.623-7C>G
|
|
|
NM_001033859.2:c.557-7C>G
|
NP_001029031.1:n.557-7C>G
|
|
|
NM_001270447.1:c.692-7C>G
|
NP_001257376.1:n.692-7C>G
|
|
|
NM_001270448.1:c.395-7C>G
|
NP_001257377.1:n.395-7C>G
|
|
|
XM_006721516.2:c.623-7C>G
|
XP_006721579.2:n.623-7C>G
|
|
|
XM_011523829.1:c.623-7C>G
|
XP_011522131.1:n.623-7C>G
|
|
|
XM_011523830.1:c.623-7C>G
|
XP_011522132.1:n.623-7C>G
|
|
|
XR_934021.1:n.730-7C>G
|
|
|
|
XR_934022.1:n.730-7C>G
|
|
|
|
XR_934023.1:n.730-7C>G
|
|
|
|
XM_006721516.3:c.623-7C>G
|
XP_006721579.2:n.623-7C>G
|
|
|
XM_011523829.2:c.623-7C>G
|
XP_011522131.1:n.623-7C>G
|
|
|
XM_011523830.2:c.623-7C>G
|
XP_011522132.1:n.623-7C>G
|
|
|
XM_024450741.1:c.623-7C>G
|
XP_024306509.1:n.623-7C>G
|
|
|
XR_934021.2:n.682-7C>G
|
|
|
|
XR_934022.2:n.682-7C>G
|
|
|
|
XR_934023.2:n.682-7C>G
|
|
|
|
NM_000018.4:c.623-7C>G
MANE Select
|
NP_000009.1:n.623-7C>G
|
|
|
NM_001033859.3:c.557-7C>G
|
NP_001029031.1:n.557-7C>G
|
|
|
NM_001270447.2:c.692-7C>G
|
NP_001257376.1:n.692-7C>G
|
|
|
NM_001270448.2:c.395-7C>G
|
NP_001257377.1:n.395-7C>G
|
|
