ENST00000452035.7:n.2100C>G
|
|
|
ENST00000483004.2:c.1492C>G
|
ENSP00000419887.2:p.Pro498Ala
|
|
ENST00000698628.1:c.1624+299C>G
|
ENSP00000513848.1:n.1624+299C>G
|
|
ENST00000698629.1:n.1885C>G
|
|
|
ENST00000698630.1:n.2424C>G
|
|
|
ENST00000698631.1:n.2425C>G
|
|
|
ENST00000698632.1:n.3219C>G
|
|
|
ENST00000698633.1:n.3109C>G
|
|
|
ENST00000698636.1:n.1930C>G
|
|
|
ENST00000425368.7:c.1708C>G
MANE Select
|
ENSP00000416561.2:p.Pro570Ala
|
|
ENST00000425368.6:c.1708C>G
|
ENSP00000416561.2:p.Pro570Ala
|
|
ENST00000456570.5:c.3214C>G
|
ENSP00000410815.1:p.Pro1072Ala
|
|
ENST00000467360.1:n.834C>G
|
|
|
ENST00000477310.1:c.2761C>G
|
ENSP00000418996.1:p.Pro921Ala
|
|
ENST00000483004.1:c.330C>G
|
|
|
NM_001710.5:c.1708C>G , LRG_136t1:c.1708C>G
|
NP_001701.2:p.Pro570Ala
|
|
NM_001710.6:c.1708C>G
MANE Select
|
NP_001701.2:p.Pro570Ala
|
|