|
ENST00000356839.10:c.1596T>A
MANE Select
|
ENSP00000349297.5:p.Ser532Arg
|
|
|
ENST00000322910.9:c.*1551T>A
|
ENSP00000325395.5:n.*1551T>A
|
|
|
ENST00000350303.9:c.1530T>A
|
ENSP00000344152.5:p.Ser510Arg
|
|
|
ENST00000356839.9:c.1596T>A
|
ENSP00000349297.5:p.Ser532Arg
|
|
|
ENST00000542255.6:c.454T>A
|
|
|
|
ENST00000543245.6:c.1665T>A
|
ENSP00000438689.2:p.Ser555Arg
|
|
|
ENST00000578319.5:n.91T>A
|
|
|
|
ENST00000578711.1:n.880T>A
|
|
|
|
ENST00000578809.5:n.168T>A
|
|
|
|
ENST00000579391.1:n.204T>A
|
|
|
|
ENST00000579425.5:n.712T>A
|
|
|
|
ENST00000579546.1:c.335T>A
|
|
|
|
ENST00000579894.5:n.383T>A
|
|
|
|
ENST00000582450.1:n.104T>A
|
|
|
|
ENST00000583074.5:n.217T>A
|
|
|
|
ENST00000583850.5:n.371T>A
|
|
|
|
ENST00000583858.5:c.527T>A
|
|
|
|
ENST00000585203.6:n.787T>A
|
|
|
|
NM_000018.3:c.1596T>A
|
NP_000009.1:p.Ser532Arg
|
|
|
NM_001033859.2:c.1530T>A
|
NP_001029031.1:p.Ser510Arg
|
|
|
NM_001270447.1:c.1665T>A
|
NP_001257376.1:p.Ser555Arg
|
|
|
NM_001270448.1:c.1368T>A
|
NP_001257377.1:p.Ser456Arg
|
|
|
XM_006721516.2:c.1596T>A
|
XP_006721579.2:p.Ser532Arg
|
|
|
XM_011523829.1:c.1498T>A
|
XP_011522131.1:p.Trp500Arg
|
|
|
XM_011523830.1:c.1498T>A
|
XP_011522132.1:p.Trp500Arg
|
|
|
XR_934021.1:n.1703T>A
|
|
|
|
XR_934022.1:n.1605T>A
|
|
|
|
XR_934023.1:n.1605T>A
|
|
|
|
XM_006721516.3:c.1596T>A
|
XP_006721579.2:p.Ser532Arg
|
|
|
XM_011523829.2:c.1498T>A
|
XP_011522131.1:p.Trp500Arg
|
|
|
XM_011523830.2:c.1498T>A
|
XP_011522132.1:p.Trp500Arg
|
|
|
XM_024450741.1:c.1498T>A
|
XP_024306509.1:p.Trp500Arg
|
|
|
XR_934021.2:n.1655T>A
|
|
|
|
XR_934022.2:n.1557T>A
|
|
|
|
XR_934023.2:n.1557T>A
|
|
|
|
NM_000018.4:c.1596T>A
MANE Select
|
NP_000009.1:p.Ser532Arg
|
|
|
NM_001033859.3:c.1530T>A
|
NP_001029031.1:p.Ser510Arg
|
|
|
NM_001270447.2:c.1665T>A
|
NP_001257376.1:p.Ser555Arg
|
|
|
NM_001270448.2:c.1368T>A
|
NP_001257377.1:p.Ser456Arg
|
|
