|
ENST00000356839.10:c.1679A>C
MANE Select
|
ENSP00000349297.5:p.Asn560Thr
|
|
|
ENST00000322910.9:c.*1634A>C
|
ENSP00000325395.5:n.*1634A>C
|
|
|
ENST00000350303.9:c.1613A>C
|
ENSP00000344152.5:p.Asn538Thr
|
|
|
ENST00000356839.9:c.1679A>C
|
ENSP00000349297.5:p.Asn560Thr
|
|
|
ENST00000542255.6:c.537-73A>C
|
|
|
|
ENST00000543245.6:c.1748A>C
|
ENSP00000438689.2:p.Asn583Thr
|
|
|
ENST00000578033.1:n.10A>C
|
|
|
|
ENST00000578319.5:n.260A>C
|
|
|
|
ENST00000578711.1:n.1138A>C
|
|
|
|
ENST00000578809.5:n.251A>C
|
|
|
|
ENST00000579425.5:n.795A>C
|
|
|
|
ENST00000579546.1:c.414A>C
|
|
|
|
ENST00000582450.1:n.276A>C
|
|
|
|
ENST00000583074.5:n.300-73A>C
|
|
|
|
ENST00000583848.5:c.65-20A>C
|
ENSP00000466487.1:n.65-20A>C
|
|
|
ENST00000583850.5:n.450A>C
|
|
|
|
ENST00000583858.5:c.610A>C
|
|
|
|
ENST00000585203.6:n.870A>C
|
|
|
|
NM_000018.3:c.1679A>C
|
NP_000009.1:p.Asn560Thr
|
|
|
NM_001033859.2:c.1613A>C
|
NP_001029031.1:p.Asn538Thr
|
|
|
NM_001270447.1:c.1748A>C
|
NP_001257376.1:p.Asn583Thr
|
|
|
NM_001270448.1:c.1451A>C
|
NP_001257377.1:p.Asn484Thr
|
|
|
XM_006721516.2:c.1679-73A>C
|
XP_006721579.2:n.1679-73A>C
|
|
|
XM_011523829.1:c.1577-73A>C
|
XP_011522131.1:n.1577-73A>C
|
|
|
XM_011523830.1:c.1577A>C
|
XP_011522132.1:p.Asn526Thr
|
|
|
XR_934021.1:n.1782A>C
|
|
|
|
XR_934022.1:n.1688A>C
|
|
|
|
XR_934023.1:n.1688-73A>C
|
|
|
|
XM_006721516.3:c.1679-73A>C
|
XP_006721579.2:n.1679-73A>C
|
|
|
XM_011523829.2:c.1577-73A>C
|
XP_011522131.1:n.1577-73A>C
|
|
|
XM_011523830.2:c.1577A>C
|
XP_011522132.1:p.Asn526Thr
|
|
|
XM_024450741.1:c.1667A>C
|
XP_024306509.1:p.Asn556Thr
|
|
|
XR_934021.2:n.1734A>C
|
|
|
|
XR_934022.2:n.1640A>C
|
|
|
|
XR_934023.2:n.1640-73A>C
|
|
|
|
NM_000018.4:c.1679A>C
MANE Select
|
NP_000009.1:p.Asn560Thr
|
|
|
NM_001033859.3:c.1613A>C
|
NP_001029031.1:p.Asn538Thr
|
|
|
NM_001270447.2:c.1748A>C
|
NP_001257376.1:p.Asn583Thr
|
|
|
NM_001270448.2:c.1451A>C
|
NP_001257377.1:p.Asn484Thr
|
|
