ENST00000398603.6:c.337-236C>A
|
ENSP00000381604.1:n.337-236C>A
|
|
ENST00000398606.10:c.386C>A
MANE Select
|
ENSP00000381607.3:p.Pro129His
|
|
ENST00000646888.1:c.*102C>A
|
ENSP00000494477.1:n.*102C>A
|
|
ENST00000398603.5:c.337-236C>A
|
ENSP00000381604.1:n.337-236C>A
|
|
ENST00000398606.7:c.386C>A
|
ENSP00000381607.3:p.Pro129His
|
|
ENST00000467591.1:n.497C>A
|
|
|
ENST00000494593.1:n.1181C>A
|
|
|
ENST00000495996.1:c.50C>A
|
ENSP00000484686.1:p.Pro17His
|
|
ENST00000498765.5:c.449C>A
|
|
|
NM_000852.3:c.386C>A , LRG_723t1:c.386C>A
|
NP_000843.1:p.Pro129His
|
|
NM_000852.4:c.386C>A
MANE Select
|
NP_000843.1:p.Pro129His
|
|