ENST00000328300.11:c.4166A>C
MANE Select
|
ENSP00000331902.7:p.Gln1389Pro
|
|
ENST00000361603.7:c.4148A>C
|
ENSP00000354505.2:p.Gln1383Pro
|
|
ENST00000510690.2:n.660A>C
|
|
|
ENST00000328300.10:c.4166A>C
|
ENSP00000331902.6:p.Gln1389Pro
|
|
ENST00000361603.6:c.4148A>C
|
ENSP00000354505.2:p.Gln1383Pro
|
|
ENST00000489230.1:n.569A>C
|
|
|
NM_000495.4:c.4148A>C
|
NP_000486.1:p.Gln1383Pro
|
|
NM_033380.2:c.4166A>C
|
NP_203699.1:p.Gln1389Pro
|
|
XM_005262070.2:c.4157A>C
|
XP_005262127.1:p.Gln1386Pro
|
|
XM_006724616.2:c.4166A>C
|
XP_006724679.1:p.Gln1389Pro
|
|
XM_011530849.1:c.3842A>C
|
XP_011529151.1:p.Gln1281Pro
|
|
XM_011530851.1:c.1739A>C
|
XP_011529153.1:p.Gln580Pro
|
|
XM_011530849.2:c.4181A>C
|
XP_011529151.2:p.Gln1394Pro
|
|
XM_017029259.2:c.4172A>C
|
XP_016884748.1:p.Gln1391Pro
|
|
XM_017029260.1:c.4163A>C
|
XP_016884749.1:p.Gln1388Pro
|
|
XM_017029263.2:c.2501A>C
|
XP_016884752.1:p.Gln834Pro
|
|
NM_000495.5:c.4148A>C
|
NP_000486.1:p.Gln1383Pro
|
|
NM_033380.3:c.4166A>C
MANE Select
|
NP_203699.1:p.Gln1389Pro
|
|