ENST00000328300.11:c.4415G>C
MANE Select
|
ENSP00000331902.7:p.Arg1472Pro
|
|
ENST00000361603.7:c.4397G>C
|
ENSP00000354505.2:p.Arg1466Pro
|
|
ENST00000510690.2:n.909G>C
|
|
|
ENST00000328300.10:c.4415G>C
|
ENSP00000331902.6:p.Arg1472Pro
|
|
ENST00000361603.6:c.4397G>C
|
ENSP00000354505.2:p.Arg1466Pro
|
|
ENST00000515658.1:c.211G>C
|
|
|
NM_000495.4:c.4397G>C
|
NP_000486.1:p.Arg1466Pro
|
|
NM_033380.2:c.4415G>C
|
NP_203699.1:p.Arg1472Pro
|
|
XM_005262070.2:c.4406G>C
|
XP_005262127.1:p.Arg1469Pro
|
|
XM_006724616.2:c.4415G>C
|
XP_006724679.1:p.Arg1472Pro
|
|
XM_011530849.1:c.4091G>C
|
XP_011529151.1:p.Arg1364Pro
|
|
XM_011530851.1:c.1988G>C
|
XP_011529153.1:p.Arg663Pro
|
|
XM_011530849.2:c.4430G>C
|
XP_011529151.2:p.Arg1477Pro
|
|
XM_017029259.2:c.4421G>C
|
XP_016884748.1:p.Arg1474Pro
|
|
XM_017029260.1:c.4412G>C
|
XP_016884749.1:p.Arg1471Pro
|
|
XM_017029263.2:c.2750G>C
|
XP_016884752.1:p.Arg917Pro
|
|
NM_000495.5:c.4397G>C
|
NP_000486.1:p.Arg1466Pro
|
|
NM_033380.3:c.4415G>C
MANE Select
|
NP_203699.1:p.Arg1472Pro
|
|