ENST00000328300.11:c.4082C>A
MANE Select
|
ENSP00000331902.7:p.Pro1361His
|
|
ENST00000361603.7:c.4064C>A
|
ENSP00000354505.2:p.Pro1355His
|
|
ENST00000510690.2:n.576C>A
|
|
|
ENST00000328300.10:c.4082C>A
|
ENSP00000331902.6:p.Pro1361His
|
|
ENST00000361603.6:c.4064C>A
|
ENSP00000354505.2:p.Pro1355His
|
|
ENST00000489230.1:n.485C>A
|
|
|
NM_000495.4:c.4064C>A
|
NP_000486.1:p.Pro1355His
|
|
NM_033380.2:c.4082C>A
|
NP_203699.1:p.Pro1361His
|
|
XM_005262070.2:c.4073C>A
|
XP_005262127.1:p.Pro1358His
|
|
XM_006724616.2:c.4082C>A
|
XP_006724679.1:p.Pro1361His
|
|
XM_011530849.1:c.3758C>A
|
XP_011529151.1:p.Pro1253His
|
|
XM_011530851.1:c.1655C>A
|
XP_011529153.1:p.Pro552His
|
|
XM_011530849.2:c.4097C>A
|
XP_011529151.2:p.Pro1366His
|
|
XM_017029259.2:c.4088C>A
|
XP_016884748.1:p.Pro1363His
|
|
XM_017029260.1:c.4079C>A
|
XP_016884749.1:p.Pro1360His
|
|
XM_017029263.2:c.2417C>A
|
XP_016884752.1:p.Pro806His
|
|
NM_000495.5:c.4064C>A
|
NP_000486.1:p.Pro1355His
|
|
NM_033380.3:c.4082C>A
MANE Select
|
NP_203699.1:p.Pro1361His
|
|