ENST00000267163.6:c.2605C>G
MANE Select
|
ENSP00000267163.4:p.Pro869Ala
|
|
ENST00000643064.1:c.194+95342C>G
|
|
|
ENST00000650461.1:c.2605C>G
|
ENSP00000497193.1:p.Pro869Ala
|
|
ENST00000267163.4:c.2605C>G
|
ENSP00000267163.4:p.Pro869Ala
|
|
ENST00000484879.1:n.339C>G
|
|
|
ENST00000531171.5:n.208C>G
|
|
|
NM_000321.2:c.2605C>G , LRG_517t1:c.2605C>G
|
NP_000312.2:p.Pro869Ala
|
|
XM_011535171.1:c.2344C>G
|
XP_011533473.1:p.Pro782Ala
|
|
XM_011535171.2:c.2344C>G
|
XP_011533473.1:p.Pro782Ala
|
|
NM_000321.3:c.2605C>G
MANE Select
|
NP_000312.2:p.Pro869Ala
|
|