ENST00000356839.10:c.1554C>T
MANE Select
|
ENSP00000349297.5:p.Gly518=
|
|
ENST00000322910.9:c.*1509C>T
|
ENSP00000325395.5:n.*1509C>T
|
|
ENST00000350303.9:c.1488C>T
|
ENSP00000344152.5:p.Gly496=
|
|
ENST00000356839.9:c.1554C>T
|
ENSP00000349297.5:p.Gly518=
|
|
ENST00000542255.6:c.412C>T
|
|
|
ENST00000543245.6:c.1623C>T
|
ENSP00000438689.2:p.Gly541=
|
|
ENST00000578319.5:n.49C>T
|
|
|
ENST00000578711.1:n.838C>T
|
|
|
ENST00000578809.5:n.126C>T
|
|
|
ENST00000579391.1:n.162C>T
|
|
|
ENST00000579425.5:n.670C>T
|
|
|
ENST00000579546.1:c.293C>T
|
|
|
ENST00000579894.5:n.341C>T
|
|
|
ENST00000582450.1:n.62C>T
|
|
|
ENST00000583074.5:n.175C>T
|
|
|
ENST00000583850.5:n.329C>T
|
|
|
ENST00000583858.5:c.485C>T
|
|
|
ENST00000585203.6:n.745C>T
|
|
|
NM_000018.3:c.1554C>T
|
NP_000009.1:p.Gly518=
|
|
NM_001033859.2:c.1488C>T
|
NP_001029031.1:p.Gly496=
|
|
NM_001270447.1:c.1623C>T
|
NP_001257376.1:p.Gly541=
|
|
NM_001270448.1:c.1326C>T
|
NP_001257377.1:p.Gly442=
|
|
XM_006721516.2:c.1554C>T
|
XP_006721579.2:p.Gly518=
|
|
XM_011523829.1:c.1456C>T
|
XP_011522131.1:p.Pro486Ser
|
|
XM_011523830.1:c.1456C>T
|
XP_011522132.1:p.Pro486Ser
|
|
XR_934021.1:n.1661C>T
|
|
|
XR_934022.1:n.1563C>T
|
|
|
XR_934023.1:n.1563C>T
|
|
|
XM_006721516.3:c.1554C>T
|
XP_006721579.2:p.Gly518=
|
|
XM_011523829.2:c.1456C>T
|
XP_011522131.1:p.Pro486Ser
|
|
XM_011523830.2:c.1456C>T
|
XP_011522132.1:p.Pro486Ser
|
|
XM_024450741.1:c.1456C>T
|
XP_024306509.1:p.Pro486Ser
|
|
XR_934021.2:n.1613C>T
|
|
|
XR_934022.2:n.1515C>T
|
|
|
XR_934023.2:n.1515C>T
|
|
|
NM_000018.4:c.1554C>T
MANE Select
|
NP_000009.1:p.Gly518=
|
|
NM_001033859.3:c.1488C>T
|
NP_001029031.1:p.Gly496=
|
|
NM_001270447.2:c.1623C>T
|
NP_001257376.1:p.Gly541=
|
|
NM_001270448.2:c.1326C>T
|
NP_001257377.1:p.Gly442=
|
|