|
ENST00000356839.10:c.1679-13A>G
MANE Select
|
ENSP00000349297.5:n.1679-13A>G
|
|
|
ENST00000322910.9:c.*1634-13A>G
|
ENSP00000325395.5:n.*1634-13A>G
|
|
|
ENST00000350303.9:c.1613-13A>G
|
ENSP00000344152.5:n.1613-13A>G
|
|
|
ENST00000356839.9:c.1679-13A>G
|
ENSP00000349297.5:n.1679-13A>G
|
|
|
ENST00000542255.6:c.536+77A>G
|
|
|
|
ENST00000543245.6:c.1748-13A>G
|
ENSP00000438689.2:n.1748-13A>G
|
|
|
ENST00000578319.5:n.260-13A>G
|
|
|
|
ENST00000578711.1:n.1125A>G
|
|
|
|
ENST00000578809.5:n.251-13A>G
|
|
|
|
ENST00000579425.5:n.795-13A>G
|
|
|
|
ENST00000579546.1:c.414-13A>G
|
|
|
|
ENST00000582450.1:n.263A>G
|
|
|
|
ENST00000583074.5:n.299+77A>G
|
|
|
|
ENST00000583848.5:c.65-33A>G
|
ENSP00000466487.1:n.65-33A>G
|
|
|
ENST00000583850.5:n.450-13A>G
|
|
|
|
ENST00000583858.5:c.610-13A>G
|
|
|
|
ENST00000585203.6:n.870-13A>G
|
|
|
|
NM_000018.3:c.1679-13A>G
|
NP_000009.1:n.1679-13A>G
|
|
|
NM_001033859.2:c.1613-13A>G
|
NP_001029031.1:n.1613-13A>G
|
|
|
NM_001270447.1:c.1748-13A>G
|
NP_001257376.1:n.1748-13A>G
|
|
|
NM_001270448.1:c.1451-13A>G
|
NP_001257377.1:n.1451-13A>G
|
|
|
XM_006721516.2:c.1678+77A>G
|
XP_006721579.2:n.1678+77A>G
|
|
|
XM_011523829.1:c.1576+77A>G
|
XP_011522131.1:n.1576+77A>G
|
|
|
XM_011523830.1:c.1577-13A>G
|
XP_011522132.1:n.1577-13A>G
|
|
|
XR_934021.1:n.1782-13A>G
|
|
|
|
XR_934022.1:n.1688-13A>G
|
|
|
|
XR_934023.1:n.1687+77A>G
|
|
|
|
XM_006721516.3:c.1678+77A>G
|
XP_006721579.2:n.1678+77A>G
|
|
|
XM_011523829.2:c.1576+77A>G
|
XP_011522131.1:n.1576+77A>G
|
|
|
XM_011523830.2:c.1577-13A>G
|
XP_011522132.1:n.1577-13A>G
|
|
|
XM_024450741.1:c.1667-13A>G
|
XP_024306509.1:n.1667-13A>G
|
|
|
XR_934021.2:n.1734-13A>G
|
|
|
|
XR_934022.2:n.1640-13A>G
|
|
|
|
XR_934023.2:n.1639+77A>G
|
|
|
|
NM_000018.4:c.1679-13A>G
MANE Select
|
NP_000009.1:n.1679-13A>G
|
|
|
NM_001033859.3:c.1613-13A>G
|
NP_001029031.1:n.1613-13A>G
|
|
|
NM_001270447.2:c.1748-13A>G
|
NP_001257376.1:n.1748-13A>G
|
|
|
NM_001270448.2:c.1451-13A>G
|
NP_001257377.1:n.1451-13A>G
|
|
