|
ENST00000356839.10:c.1752-34C>G
MANE Select
|
ENSP00000349297.5:n.1752-34C>G
|
|
|
ENST00000322910.9:c.*1707-34C>G
|
ENSP00000325395.5:n.*1707-34C>G
|
|
|
ENST00000350303.9:c.1686-34C>G
|
ENSP00000344152.5:n.1686-34C>G
|
|
|
ENST00000356839.9:c.1752-34C>G
|
ENSP00000349297.5:n.1752-34C>G
|
|
|
ENST00000542255.6:c.597C>G
|
|
|
|
ENST00000543245.6:c.1821-34C>G
|
ENSP00000438689.2:n.1821-34C>G
|
|
|
ENST00000578033.1:n.143C>G
|
|
|
|
ENST00000578319.5:n.333-34C>G
|
|
|
|
ENST00000578711.1:n.1271C>G
|
|
|
|
ENST00000578809.5:n.324-34C>G
|
|
|
|
ENST00000579425.5:n.868-34C>G
|
|
|
|
ENST00000579546.1:c.487-34C>G
|
|
|
|
ENST00000583074.5:n.360C>G
|
|
|
|
ENST00000583848.5:c.118-34C>G
|
ENSP00000466487.1:n.118-34C>G
|
|
|
ENST00000583850.5:n.523-34C>G
|
|
|
|
ENST00000583858.5:c.683-34C>G
|
|
|
|
ENST00000585203.6:n.943-34C>G
|
|
|
|
NM_000018.3:c.1752-34C>G
|
NP_000009.1:n.1752-34C>G
|
|
|
NM_001033859.2:c.1686-34C>G
|
NP_001029031.1:n.1686-34C>G
|
|
|
NM_001270447.1:c.1821-34C>G
|
NP_001257376.1:n.1821-34C>G
|
|
|
NM_001270448.1:c.1524-34C>G
|
NP_001257377.1:n.1524-34C>G
|
|
|
XM_006721516.2:c.1739C>G
|
XP_006721579.2:p.Ala580Gly
|
|
|
XM_011523829.1:c.1637C>G
|
XP_011522131.1:p.Ala546Gly
|
|
|
XM_011523830.1:c.1650-34C>G
|
XP_011522132.1:n.1650-34C>G
|
|
|
XR_934021.1:n.1855-34C>G
|
|
|
|
XR_934022.1:n.1761-34C>G
|
|
|
|
XR_934023.1:n.1748C>G
|
|
|
|
XM_006721516.3:c.1739C>G
|
XP_006721579.2:p.Ala580Gly
|
|
|
XM_011523829.2:c.1637C>G
|
XP_011522131.1:p.Ala546Gly
|
|
|
XM_011523830.2:c.1650-34C>G
|
XP_011522132.1:n.1650-34C>G
|
|
|
XM_024450741.1:c.1740-34C>G
|
XP_024306509.1:n.1740-34C>G
|
|
|
XR_934021.2:n.1807-34C>G
|
|
|
|
XR_934022.2:n.1713-34C>G
|
|
|
|
XR_934023.2:n.1700C>G
|
|
|
|
NM_000018.4:c.1752-34C>G
MANE Select
|
NP_000009.1:n.1752-34C>G
|
|
|
NM_001033859.3:c.1686-34C>G
|
NP_001029031.1:n.1686-34C>G
|
|
|
NM_001270447.2:c.1821-34C>G
|
NP_001257376.1:n.1821-34C>G
|
|
|
NM_001270448.2:c.1524-34C>G
|
NP_001257377.1:n.1524-34C>G
|
|
