|
ENST00000356839.10:c.1533G>A
MANE Select
|
ENSP00000349297.5:p.Arg511=
|
|
|
ENST00000322910.9:c.*1488G>A
|
ENSP00000325395.5:n.*1488G>A
|
|
|
ENST00000350303.9:c.1467G>A
|
ENSP00000344152.5:p.Arg489=
|
|
|
ENST00000356839.9:c.1533G>A
|
ENSP00000349297.5:p.Arg511=
|
|
|
ENST00000542255.6:c.391G>A
|
|
|
|
ENST00000543245.6:c.1602G>A
|
ENSP00000438689.2:p.Arg534=
|
|
|
ENST00000578319.5:n.28G>A
|
|
|
|
ENST00000578711.1:n.817G>A
|
|
|
|
ENST00000578809.5:n.105G>A
|
|
|
|
ENST00000579391.1:n.141G>A
|
|
|
|
ENST00000579425.5:n.649G>A
|
|
|
|
ENST00000579546.1:c.272G>A
|
|
|
|
ENST00000579894.5:n.320G>A
|
|
|
|
ENST00000582450.1:n.41G>A
|
|
|
|
ENST00000583074.5:n.154G>A
|
|
|
|
ENST00000583850.5:n.308G>A
|
|
|
|
ENST00000583858.5:c.464G>A
|
|
|
|
ENST00000585203.6:n.724G>A
|
|
|
|
NM_000018.3:c.1533G>A
|
NP_000009.1:p.Arg511=
|
|
|
NM_001033859.2:c.1467G>A
|
NP_001029031.1:p.Arg489=
|
|
|
NM_001270447.1:c.1602G>A
|
NP_001257376.1:p.Arg534=
|
|
|
NM_001270448.1:c.1305G>A
|
NP_001257377.1:p.Arg435=
|
|
|
XM_006721516.2:c.1533G>A
|
XP_006721579.2:p.Arg511=
|
|
|
XM_011523829.1:c.1435G>A
|
XP_011522131.1:p.Ala479Thr
|
|
|
XM_011523830.1:c.1435G>A
|
XP_011522132.1:p.Ala479Thr
|
|
|
XR_934021.1:n.1640G>A
|
|
|
|
XR_934022.1:n.1542G>A
|
|
|
|
XR_934023.1:n.1542G>A
|
|
|
|
XM_006721516.3:c.1533G>A
|
XP_006721579.2:p.Arg511=
|
|
|
XM_011523829.2:c.1435G>A
|
XP_011522131.1:p.Ala479Thr
|
|
|
XM_011523830.2:c.1435G>A
|
XP_011522132.1:p.Ala479Thr
|
|
|
XM_024450741.1:c.1435G>A
|
XP_024306509.1:p.Ala479Thr
|
|
|
XR_934021.2:n.1592G>A
|
|
|
|
XR_934022.2:n.1494G>A
|
|
|
|
XR_934023.2:n.1494G>A
|
|
|
|
NM_000018.4:c.1533G>A
MANE Select
|
NP_000009.1:p.Arg511=
|
|
|
NM_001033859.3:c.1467G>A
|
NP_001029031.1:p.Arg489=
|
|
|
NM_001270447.2:c.1602G>A
|
NP_001257376.1:p.Arg534=
|
|
|
NM_001270448.2:c.1305G>A
|
NP_001257377.1:p.Arg435=
|
|
