|
ENST00000356839.10:c.1586T>C
MANE Select
|
ENSP00000349297.5:p.Leu529Ser
|
|
|
ENST00000322910.9:c.*1541T>C
|
ENSP00000325395.5:n.*1541T>C
|
|
|
ENST00000350303.9:c.1520T>C
|
ENSP00000344152.5:p.Leu507Ser
|
|
|
ENST00000356839.9:c.1586T>C
|
ENSP00000349297.5:p.Leu529Ser
|
|
|
ENST00000542255.6:c.444T>C
|
|
|
|
ENST00000543245.6:c.1655T>C
|
ENSP00000438689.2:p.Leu552Ser
|
|
|
ENST00000578319.5:n.81T>C
|
|
|
|
ENST00000578711.1:n.870T>C
|
|
|
|
ENST00000578809.5:n.158T>C
|
|
|
|
ENST00000579391.1:n.194T>C
|
|
|
|
ENST00000579425.5:n.702T>C
|
|
|
|
ENST00000579546.1:c.325T>C
|
|
|
|
ENST00000579894.5:n.373T>C
|
|
|
|
ENST00000582450.1:n.94T>C
|
|
|
|
ENST00000583074.5:n.207T>C
|
|
|
|
ENST00000583850.5:n.361T>C
|
|
|
|
ENST00000583858.5:c.517T>C
|
|
|
|
ENST00000585203.6:n.777T>C
|
|
|
|
NM_000018.3:c.1586T>C
|
NP_000009.1:p.Leu529Ser
|
|
|
NM_001033859.2:c.1520T>C
|
NP_001029031.1:p.Leu507Ser
|
|
|
NM_001270447.1:c.1655T>C
|
NP_001257376.1:p.Leu552Ser
|
|
|
NM_001270448.1:c.1358T>C
|
NP_001257377.1:p.Leu453Ser
|
|
|
XM_006721516.2:c.1586T>C
|
XP_006721579.2:p.Leu529Ser
|
|
|
XM_011523829.1:c.1488T>C
|
XP_011522131.1:p.Val496=
|
|
|
XM_011523830.1:c.1488T>C
|
XP_011522132.1:p.Val496=
|
|
|
XR_934021.1:n.1693T>C
|
|
|
|
XR_934022.1:n.1595T>C
|
|
|
|
XR_934023.1:n.1595T>C
|
|
|
|
XM_006721516.3:c.1586T>C
|
XP_006721579.2:p.Leu529Ser
|
|
|
XM_011523829.2:c.1488T>C
|
XP_011522131.1:p.Val496=
|
|
|
XM_011523830.2:c.1488T>C
|
XP_011522132.1:p.Val496=
|
|
|
XM_024450741.1:c.1488T>C
|
XP_024306509.1:p.Val496=
|
|
|
XR_934021.2:n.1645T>C
|
|
|
|
XR_934022.2:n.1547T>C
|
|
|
|
XR_934023.2:n.1547T>C
|
|
|
|
NM_000018.4:c.1586T>C
MANE Select
|
NP_000009.1:p.Leu529Ser
|
|
|
NM_001033859.3:c.1520T>C
|
NP_001029031.1:p.Leu507Ser
|
|
|
NM_001270447.2:c.1655T>C
|
NP_001257376.1:p.Leu552Ser
|
|
|
NM_001270448.2:c.1358T>C
|
NP_001257377.1:p.Leu453Ser
|
|
