ENST00000502274.2:c.797C>G
|
|
|
ENST00000515425.6:c.907C>G
MANE Select
|
ENSP00000423660.1:p.Pro303Ala
|
|
ENST00000674655.1:c.169C>G
|
ENSP00000502840.1:p.Pro57Ala
|
|
ENST00000674983.1:c.*165C>G
|
ENSP00000502387.1:n.*165C>G
|
|
ENST00000675793.1:c.907C>G
|
ENSP00000502039.1:p.Pro303Ala
|
|
ENST00000676056.1:c.*165C>G
|
ENSP00000501827.1:n.*165C>G
|
|
ENST00000323829.9:c.*165C>G
|
ENSP00000313025.5:n.*165C>G
|
|
ENST00000503071.1:n.374C>G
|
|
|
ENST00000504517.5:c.307C>G
|
ENSP00000421779.1:p.Pro103Ala
|
|
ENST00000504690.5:c.907C>G
|
ENSP00000425627.1:p.Pro303Ala
|
|
ENST00000511307.5:c.*687C>G
|
ENSP00000421420.1:n.*687C>G
|
|
ENST00000512049.5:c.886C>G
|
ENSP00000421860.1:p.Pro296Ala
|
|
ENST00000513604.5:c.*165C>G
|
ENSP00000423111.1:n.*165C>G
|
|
ENST00000515425.5:c.907C>G
|
ENSP00000423660.1:p.Pro303Ala
|
|
NM_024577.3:c.907C>G , LRG_269t1:c.907C>G
|
NP_078853.2:p.Pro303Ala
|
|
NM_024577.4:c.907C>G
MANE Select
|
NP_078853.2:p.Pro303Ala
|
|