ENST00000372748.8:c.1963C>G
MANE Select
|
ENSP00000361834.3:p.Pro655Ala
|
|
ENST00000372748.7:c.1963C>G
|
ENSP00000361834.3:p.Pro655Ala
|
|
ENST00000482722.5:n.2266C>G
|
|
|
NM_001852.3:c.1963C>G
|
NP_001843.1:p.Pro655Ala
|
|
XM_006710365.2:c.1963C>G
|
XP_006710428.1:p.Pro655Ala
|
|
XM_011540714.1:c.1975C>G
|
XP_011539016.1:p.Pro659Ala
|
|
XM_011540715.1:c.1693C>G
|
XP_011539017.1:p.Pro565Ala
|
|
XM_011540716.1:c.1693C>G
|
XP_011539018.1:p.Pro565Ala
|
|
XM_011540717.1:c.1420C>G
|
XP_011539019.1:p.Pro474Ala
|
|
XM_006710365.3:c.1963C>G
|
XP_006710428.1:p.Pro655Ala
|
|
XM_011540715.2:c.1693C>G
|
XP_011539017.1:p.Pro565Ala
|
|
XM_011540716.2:c.1693C>G
|
XP_011539018.1:p.Pro565Ala
|
|
XM_011540717.2:c.1420C>G
|
XP_011539019.1:p.Pro474Ala
|
|
XM_017000332.1:c.1975C>G
|
XP_016855821.1:p.Pro659Ala
|
|
XM_017000333.1:c.1681C>G
|
XP_016855822.1:p.Pro561Ala
|
|
NM_001852.4:c.1963C>G
MANE Select
|
NP_001843.1:p.Pro655Ala
|
|