|
ENST00000356839.10:c.1685A>C
MANE Select
|
ENSP00000349297.5:p.Gln562Pro
|
|
|
ENST00000322910.9:c.*1640A>C
|
ENSP00000325395.5:n.*1640A>C
|
|
|
ENST00000350303.9:c.1619A>C
|
ENSP00000344152.5:p.Gln540Pro
|
|
|
ENST00000356839.9:c.1685A>C
|
ENSP00000349297.5:p.Gln562Pro
|
|
|
ENST00000542255.6:c.537-67A>C
|
|
|
|
ENST00000543245.6:c.1754A>C
|
ENSP00000438689.2:p.Gln585Pro
|
|
|
ENST00000578033.1:n.16A>C
|
|
|
|
ENST00000578319.5:n.266A>C
|
|
|
|
ENST00000578711.1:n.1144A>C
|
|
|
|
ENST00000578809.5:n.257A>C
|
|
|
|
ENST00000579425.5:n.801A>C
|
|
|
|
ENST00000579546.1:c.420A>C
|
|
|
|
ENST00000582450.1:n.282A>C
|
|
|
|
ENST00000583074.5:n.300-67A>C
|
|
|
|
ENST00000583848.5:c.65-14A>C
|
ENSP00000466487.1:n.65-14A>C
|
|
|
ENST00000583850.5:n.456A>C
|
|
|
|
ENST00000583858.5:c.616A>C
|
|
|
|
ENST00000585203.6:n.876A>C
|
|
|
|
NM_000018.3:c.1685A>C
|
NP_000009.1:p.Gln562Pro
|
|
|
NM_001033859.2:c.1619A>C
|
NP_001029031.1:p.Gln540Pro
|
|
|
NM_001270447.1:c.1754A>C
|
NP_001257376.1:p.Gln585Pro
|
|
|
NM_001270448.1:c.1457A>C
|
NP_001257377.1:p.Gln486Pro
|
|
|
XM_006721516.2:c.1679-67A>C
|
XP_006721579.2:n.1679-67A>C
|
|
|
XM_011523829.1:c.1577-67A>C
|
XP_011522131.1:n.1577-67A>C
|
|
|
XM_011523830.1:c.1583A>C
|
XP_011522132.1:p.Gln528Pro
|
|
|
XR_934021.1:n.1788A>C
|
|
|
|
XR_934022.1:n.1694A>C
|
|
|
|
XR_934023.1:n.1688-67A>C
|
|
|
|
XM_006721516.3:c.1679-67A>C
|
XP_006721579.2:n.1679-67A>C
|
|
|
XM_011523829.2:c.1577-67A>C
|
XP_011522131.1:n.1577-67A>C
|
|
|
XM_011523830.2:c.1583A>C
|
XP_011522132.1:p.Gln528Pro
|
|
|
XM_024450741.1:c.1673A>C
|
XP_024306509.1:p.Gln558Pro
|
|
|
XR_934021.2:n.1740A>C
|
|
|
|
XR_934022.2:n.1646A>C
|
|
|
|
XR_934023.2:n.1640-67A>C
|
|
|
|
NM_000018.4:c.1685A>C
MANE Select
|
NP_000009.1:p.Gln562Pro
|
|
|
NM_001033859.3:c.1619A>C
|
NP_001029031.1:p.Gln540Pro
|
|
|
NM_001270447.2:c.1754A>C
|
NP_001257376.1:p.Gln585Pro
|
|
|
NM_001270448.2:c.1457A>C
|
NP_001257377.1:p.Gln486Pro
|
|
