ENST00000270357.10:c.1546C>T
MANE Select
|
ENSP00000270357.4:p.Pro516Ser
|
|
ENST00000270357.8:c.853C>T
|
ENSP00000270357.3:p.Pro285Ser
|
|
ENST00000437406.1:c.112C>T
|
ENSP00000403319.1:p.Pro38Ser
|
|
ENST00000451363.5:c.187C>T
|
ENSP00000414661.1:p.Pro63Ser
|
|
ENST00000464550.5:n.382C>T
|
|
|
ENST00000471657.1:n.349C>T
|
|
|
ENST00000481757.5:n.2480C>T
|
|
|
ENST00000486058.5:n.1659C>T
|
|
|
ENST00000493398.5:n.692C>T
|
|
|
NM_018226.4:c.1546C>T
|
NP_060696.4:p.Pro516Ser
|
|
XM_005247036.3:c.1513C>T
|
XP_005247093.1:p.Pro505Ser
|
|
NM_018226.5:c.1546C>T
|
NP_060696.4:p.Pro516Ser
|
|
XM_005247036.4:c.1513C>T
|
XP_005247093.1:p.Pro505Ser
|
|
NM_018226.6:c.1546C>T
MANE Select
|
NP_060696.4:p.Pro516Ser
|
|