ENST00000356839.10:c.1727A>C
MANE Select
|
ENSP00000349297.5:p.Tyr576Ser
|
|
ENST00000322910.9:c.*1682A>C
|
ENSP00000325395.5:n.*1682A>C
|
|
ENST00000350303.9:c.1661A>C
|
ENSP00000344152.5:p.Tyr554Ser
|
|
ENST00000356839.9:c.1727A>C
|
ENSP00000349297.5:p.Tyr576Ser
|
|
ENST00000542255.6:c.537-25A>C
|
|
|
ENST00000543245.6:c.1796A>C
|
ENSP00000438689.2:p.Tyr599Ser
|
|
ENST00000578033.1:n.58A>C
|
|
|
ENST00000578319.5:n.308A>C
|
|
|
ENST00000578711.1:n.1186A>C
|
|
|
ENST00000578809.5:n.299A>C
|
|
|
ENST00000579425.5:n.843A>C
|
|
|
ENST00000579546.1:c.462A>C
|
|
|
ENST00000583074.5:n.300-25A>C
|
|
|
ENST00000583848.5:c.93A>C
|
ENSP00000466487.1:p.Leu31=
|
|
ENST00000583850.5:n.498A>C
|
|
|
ENST00000583858.5:c.658A>C
|
|
|
ENST00000585203.6:n.918A>C
|
|
|
NM_000018.3:c.1727A>C
|
NP_000009.1:p.Tyr576Ser
|
|
NM_001033859.2:c.1661A>C
|
NP_001029031.1:p.Tyr554Ser
|
|
NM_001270447.1:c.1796A>C
|
NP_001257376.1:p.Tyr599Ser
|
|
NM_001270448.1:c.1499A>C
|
NP_001257377.1:p.Tyr500Ser
|
|
XM_006721516.2:c.1679-25A>C
|
XP_006721579.2:n.1679-25A>C
|
|
XM_011523829.1:c.1577-25A>C
|
XP_011522131.1:n.1577-25A>C
|
|
XM_011523830.1:c.1625A>C
|
XP_011522132.1:p.Tyr542Ser
|
|
XR_934021.1:n.1830A>C
|
|
|
XR_934022.1:n.1736A>C
|
|
|
XR_934023.1:n.1688-25A>C
|
|
|
XM_006721516.3:c.1679-25A>C
|
XP_006721579.2:n.1679-25A>C
|
|
XM_011523829.2:c.1577-25A>C
|
XP_011522131.1:n.1577-25A>C
|
|
XM_011523830.2:c.1625A>C
|
XP_011522132.1:p.Tyr542Ser
|
|
XM_024450741.1:c.1715A>C
|
XP_024306509.1:p.Tyr572Ser
|
|
XR_934021.2:n.1782A>C
|
|
|
XR_934022.2:n.1688A>C
|
|
|
XR_934023.2:n.1640-25A>C
|
|
|
NM_000018.4:c.1727A>C
MANE Select
|
NP_000009.1:p.Tyr576Ser
|
|
NM_001033859.3:c.1661A>C
|
NP_001029031.1:p.Tyr554Ser
|
|
NM_001270447.2:c.1796A>C
|
NP_001257376.1:p.Tyr599Ser
|
|
NM_001270448.2:c.1499A>C
|
NP_001257377.1:p.Tyr500Ser
|
|