|
ENST00000356839.10:c.1604T>G
MANE Select
|
ENSP00000349297.5:p.Leu535Arg
|
|
|
ENST00000322910.9:c.*1559T>G
|
ENSP00000325395.5:n.*1559T>G
|
|
|
ENST00000350303.9:c.1538T>G
|
ENSP00000344152.5:p.Leu513Arg
|
|
|
ENST00000356839.9:c.1604T>G
|
ENSP00000349297.5:p.Leu535Arg
|
|
|
ENST00000542255.6:c.462T>G
|
|
|
|
ENST00000543245.6:c.1673T>G
|
ENSP00000438689.2:p.Leu558Arg
|
|
|
ENST00000578319.5:n.99T>G
|
|
|
|
ENST00000578711.1:n.888T>G
|
|
|
|
ENST00000578809.5:n.176T>G
|
|
|
|
ENST00000579391.1:n.212T>G
|
|
|
|
ENST00000579425.5:n.720T>G
|
|
|
|
ENST00000579546.1:c.343T>G
|
|
|
|
ENST00000579894.5:n.391T>G
|
|
|
|
ENST00000582450.1:n.112T>G
|
|
|
|
ENST00000583074.5:n.225T>G
|
|
|
|
ENST00000583850.5:n.379T>G
|
|
|
|
ENST00000583858.5:c.535T>G
|
|
|
|
ENST00000585203.6:n.795T>G
|
|
|
|
NM_000018.3:c.1604T>G
|
NP_000009.1:p.Leu535Arg
|
|
|
NM_001033859.2:c.1538T>G
|
NP_001029031.1:p.Leu513Arg
|
|
|
NM_001270447.1:c.1673T>G
|
NP_001257376.1:p.Leu558Arg
|
|
|
NM_001270448.1:c.1376T>G
|
NP_001257377.1:p.Leu459Arg
|
|
|
XM_006721516.2:c.1604T>G
|
XP_006721579.2:p.Leu535Arg
|
|
|
XM_011523829.1:c.1506T>G
|
XP_011522131.1:p.Ala502=
|
|
|
XM_011523830.1:c.1506T>G
|
XP_011522132.1:p.Ala502=
|
|
|
XR_934021.1:n.1711T>G
|
|
|
|
XR_934022.1:n.1613T>G
|
|
|
|
XR_934023.1:n.1613T>G
|
|
|
|
XM_006721516.3:c.1604T>G
|
XP_006721579.2:p.Leu535Arg
|
|
|
XM_011523829.2:c.1506T>G
|
XP_011522131.1:p.Ala502=
|
|
|
XM_011523830.2:c.1506T>G
|
XP_011522132.1:p.Ala502=
|
|
|
XM_024450741.1:c.1506T>G
|
XP_024306509.1:p.Ala502=
|
|
|
XR_934021.2:n.1663T>G
|
|
|
|
XR_934022.2:n.1565T>G
|
|
|
|
XR_934023.2:n.1565T>G
|
|
|
|
NM_000018.4:c.1604T>G
MANE Select
|
NP_000009.1:p.Leu535Arg
|
|
|
NM_001033859.3:c.1538T>G
|
NP_001029031.1:p.Leu513Arg
|
|
|
NM_001270447.2:c.1673T>G
|
NP_001257376.1:p.Leu558Arg
|
|
|
NM_001270448.2:c.1376T>G
|
NP_001257377.1:p.Leu459Arg
|
|
