ENST00000328300.11:c.4533G>C
MANE Select
|
ENSP00000331902.7:p.Thr1511=
|
|
ENST00000361603.7:c.4515G>C
|
ENSP00000354505.2:p.Thr1505=
|
|
ENST00000510690.2:n.1027G>C
|
|
|
ENST00000328300.10:c.4533G>C
|
ENSP00000331902.6:p.Thr1511=
|
|
ENST00000361603.6:c.4515G>C
|
ENSP00000354505.2:p.Thr1505=
|
|
ENST00000515658.1:c.325-3545G>C
|
|
|
NM_000495.4:c.4515G>C
|
NP_000486.1:p.Thr1505=
|
|
NM_033380.2:c.4533G>C
|
NP_203699.1:p.Thr1511=
|
|
XM_005262070.2:c.4524G>C
|
XP_005262127.1:p.Thr1508=
|
|
XM_006724616.2:c.4533G>C
|
XP_006724679.1:p.Thr1511=
|
|
XM_011530849.1:c.4209G>C
|
XP_011529151.1:p.Thr1403=
|
|
XM_011530851.1:c.2106G>C
|
XP_011529153.1:p.Thr702=
|
|
XM_011530849.2:c.4548G>C
|
XP_011529151.2:p.Thr1516=
|
|
XM_017029259.2:c.4539G>C
|
XP_016884748.1:p.Thr1513=
|
|
XM_017029260.1:c.4530G>C
|
XP_016884749.1:p.Thr1510=
|
|
XM_017029263.2:c.2868G>C
|
XP_016884752.1:p.Thr956=
|
|
NM_000495.5:c.4515G>C
|
NP_000486.1:p.Thr1505=
|
|
NM_033380.3:c.4533G>C
MANE Select
|
NP_203699.1:p.Thr1511=
|
|