ENST00000356839.10:c.1624C>T
MANE Select
|
ENSP00000349297.5:p.Gln542Ter
|
|
ENST00000322910.9:c.*1579C>T
|
ENSP00000325395.5:n.*1579C>T
|
|
ENST00000350303.9:c.1558C>T
|
ENSP00000344152.5:p.Gln520Ter
|
|
ENST00000356839.9:c.1624C>T
|
ENSP00000349297.5:p.Gln542Ter
|
|
ENST00000542255.6:c.482C>T
|
|
|
ENST00000543245.6:c.1693C>T
|
ENSP00000438689.2:p.Gln565Ter
|
|
ENST00000578319.5:n.205C>T
|
|
|
ENST00000578711.1:n.994C>T
|
|
|
ENST00000578809.5:n.196C>T
|
|
|
ENST00000579391.1:n.228C>T
|
|
|
ENST00000579425.5:n.740C>T
|
|
|
ENST00000579546.1:c.359C>T
|
|
|
ENST00000579894.5:n.411C>T
|
|
|
ENST00000582450.1:n.132C>T
|
|
|
ENST00000583074.5:n.245C>T
|
|
|
ENST00000583848.5:c.10C>T
|
ENSP00000466487.1:p.Gln4Ter
|
|
ENST00000583850.5:n.395C>T
|
|
|
ENST00000583858.5:c.555C>T
|
|
|
ENST00000585203.6:n.815C>T
|
|
|
NM_000018.3:c.1624C>T
|
NP_000009.1:p.Gln542Ter
|
|
NM_001033859.2:c.1558C>T
|
NP_001029031.1:p.Gln520Ter
|
|
NM_001270447.1:c.1693C>T
|
NP_001257376.1:p.Gln565Ter
|
|
NM_001270448.1:c.1396C>T
|
NP_001257377.1:p.Gln466Ter
|
|
XM_006721516.2:c.1624C>T
|
XP_006721579.2:p.Gln542Ter
|
|
XM_011523829.1:c.1522C>T
|
XP_011522131.1:p.Gln508Ter
|
|
XM_011523830.1:c.1522C>T
|
XP_011522132.1:p.Gln508Ter
|
|
XR_934021.1:n.1727C>T
|
|
|
XR_934022.1:n.1633C>T
|
|
|
XR_934023.1:n.1633C>T
|
|
|
XM_006721516.3:c.1624C>T
|
XP_006721579.2:p.Gln542Ter
|
|
XM_011523829.2:c.1522C>T
|
XP_011522131.1:p.Gln508Ter
|
|
XM_011523830.2:c.1522C>T
|
XP_011522132.1:p.Gln508Ter
|
|
XM_024450741.1:c.1612C>T
|
XP_024306509.1:p.Gln538Ter
|
|
XR_934021.2:n.1679C>T
|
|
|
XR_934022.2:n.1585C>T
|
|
|
XR_934023.2:n.1585C>T
|
|
|
NM_000018.4:c.1624C>T
MANE Select
|
NP_000009.1:p.Gln542Ter
|
|
NM_001033859.3:c.1558C>T
|
NP_001029031.1:p.Gln520Ter
|
|
NM_001270447.2:c.1693C>T
|
NP_001257376.1:p.Gln565Ter
|
|
NM_001270448.2:c.1396C>T
|
NP_001257377.1:p.Gln466Ter
|
|