ENST00000328300.11:c.4304C>A
MANE Select
|
ENSP00000331902.7:p.Pro1435Gln
|
|
ENST00000361603.7:c.4286C>A
|
ENSP00000354505.2:p.Pro1429Gln
|
|
ENST00000510690.2:n.798C>A
|
|
|
ENST00000328300.10:c.4304C>A
|
ENSP00000331902.6:p.Pro1435Gln
|
|
ENST00000361603.6:c.4286C>A
|
ENSP00000354505.2:p.Pro1429Gln
|
|
ENST00000489230.1:n.707C>A
|
|
|
ENST00000515658.1:c.100C>A
|
|
|
NM_000495.4:c.4286C>A
|
NP_000486.1:p.Pro1429Gln
|
|
NM_033380.2:c.4304C>A
|
NP_203699.1:p.Pro1435Gln
|
|
XM_005262070.2:c.4295C>A
|
XP_005262127.1:p.Pro1432Gln
|
|
XM_006724616.2:c.4304C>A
|
XP_006724679.1:p.Pro1435Gln
|
|
XM_011530849.1:c.3980C>A
|
XP_011529151.1:p.Pro1327Gln
|
|
XM_011530851.1:c.1877C>A
|
XP_011529153.1:p.Pro626Gln
|
|
XM_011530849.2:c.4319C>A
|
XP_011529151.2:p.Pro1440Gln
|
|
XM_017029259.2:c.4310C>A
|
XP_016884748.1:p.Pro1437Gln
|
|
XM_017029260.1:c.4301C>A
|
XP_016884749.1:p.Pro1434Gln
|
|
XM_017029263.2:c.2639C>A
|
XP_016884752.1:p.Pro880Gln
|
|
NM_000495.5:c.4286C>A
|
NP_000486.1:p.Pro1429Gln
|
|
NM_033380.3:c.4304C>A
MANE Select
|
NP_203699.1:p.Pro1435Gln
|
|