ENST00000356839.10:c.1626G>A
MANE Select
|
ENSP00000349297.5:p.Gln542=
|
|
ENST00000322910.9:c.*1581G>A
|
ENSP00000325395.5:n.*1581G>A
|
|
ENST00000350303.9:c.1560G>A
|
ENSP00000344152.5:p.Gln520=
|
|
ENST00000356839.9:c.1626G>A
|
ENSP00000349297.5:p.Gln542=
|
|
ENST00000542255.6:c.484G>A
|
|
|
ENST00000543245.6:c.1695G>A
|
ENSP00000438689.2:p.Gln565=
|
|
ENST00000578319.5:n.207G>A
|
|
|
ENST00000578711.1:n.996G>A
|
|
|
ENST00000578809.5:n.198G>A
|
|
|
ENST00000579391.1:n.230G>A
|
|
|
ENST00000579425.5:n.742G>A
|
|
|
ENST00000579546.1:c.361G>A
|
|
|
ENST00000579894.5:n.413G>A
|
|
|
ENST00000582450.1:n.134G>A
|
|
|
ENST00000583074.5:n.247G>A
|
|
|
ENST00000583848.5:c.12G>A
|
ENSP00000466487.1:p.Gln4=
|
|
ENST00000583850.5:n.397G>A
|
|
|
ENST00000583858.5:c.557G>A
|
|
|
ENST00000585203.6:n.817G>A
|
|
|
NM_000018.3:c.1626G>A
|
NP_000009.1:p.Gln542=
|
|
NM_001033859.2:c.1560G>A
|
NP_001029031.1:p.Gln520=
|
|
NM_001270447.1:c.1695G>A
|
NP_001257376.1:p.Gln565=
|
|
NM_001270448.1:c.1398G>A
|
NP_001257377.1:p.Gln466=
|
|
XM_006721516.2:c.1626G>A
|
XP_006721579.2:p.Gln542=
|
|
XM_011523829.1:c.1524G>A
|
XP_011522131.1:p.Gln508=
|
|
XM_011523830.1:c.1524G>A
|
XP_011522132.1:p.Gln508=
|
|
XR_934021.1:n.1729G>A
|
|
|
XR_934022.1:n.1635G>A
|
|
|
XR_934023.1:n.1635G>A
|
|
|
XM_006721516.3:c.1626G>A
|
XP_006721579.2:p.Gln542=
|
|
XM_011523829.2:c.1524G>A
|
XP_011522131.1:p.Gln508=
|
|
XM_011523830.2:c.1524G>A
|
XP_011522132.1:p.Gln508=
|
|
XM_024450741.1:c.1614G>A
|
XP_024306509.1:p.Gln538=
|
|
XR_934021.2:n.1681G>A
|
|
|
XR_934022.2:n.1587G>A
|
|
|
XR_934023.2:n.1587G>A
|
|
|
NM_000018.4:c.1626G>A
MANE Select
|
NP_000009.1:p.Gln542=
|
|
NM_001033859.3:c.1560G>A
|
NP_001029031.1:p.Gln520=
|
|
NM_001270447.2:c.1695G>A
|
NP_001257376.1:p.Gln565=
|
|
NM_001270448.2:c.1398G>A
|
NP_001257377.1:p.Gln466=
|
|