ENST00000328300.11:c.4093C>G
MANE Select
|
ENSP00000331902.7:p.Pro1365Ala
|
|
ENST00000361603.7:c.4075C>G
|
ENSP00000354505.2:p.Pro1359Ala
|
|
ENST00000510690.2:n.587C>G
|
|
|
ENST00000328300.10:c.4093C>G
|
ENSP00000331902.6:p.Pro1365Ala
|
|
ENST00000361603.6:c.4075C>G
|
ENSP00000354505.2:p.Pro1359Ala
|
|
ENST00000489230.1:n.496C>G
|
|
|
NM_000495.4:c.4075C>G
|
NP_000486.1:p.Pro1359Ala
|
|
NM_033380.2:c.4093C>G
|
NP_203699.1:p.Pro1365Ala
|
|
XM_005262070.2:c.4084C>G
|
XP_005262127.1:p.Pro1362Ala
|
|
XM_006724616.2:c.4093C>G
|
XP_006724679.1:p.Pro1365Ala
|
|
XM_011530849.1:c.3769C>G
|
XP_011529151.1:p.Pro1257Ala
|
|
XM_011530851.1:c.1666C>G
|
XP_011529153.1:p.Pro556Ala
|
|
XM_011530849.2:c.4108C>G
|
XP_011529151.2:p.Pro1370Ala
|
|
XM_017029259.2:c.4099C>G
|
XP_016884748.1:p.Pro1367Ala
|
|
XM_017029260.1:c.4090C>G
|
XP_016884749.1:p.Pro1364Ala
|
|
XM_017029263.2:c.2428C>G
|
XP_016884752.1:p.Pro810Ala
|
|
NM_000495.5:c.4075C>G
|
NP_000486.1:p.Pro1359Ala
|
|
NM_033380.3:c.4093C>G
MANE Select
|
NP_203699.1:p.Pro1365Ala
|
|