ENST00000696170.1:c.*525C>A
|
ENSP00000512461.1:n.*525C>A
|
|
ENST00000696171.1:c.920C>A
|
ENSP00000512462.1:p.Pro307His
|
|
ENST00000378588.5:c.1016C>A
MANE Select
|
ENSP00000367851.4:p.Pro339His
|
|
ENST00000378588.4:c.1016C>A
|
ENSP00000367851.4:p.Pro339His
|
|
ENST00000465127.1:c.171+377995C>A
|
ENSP00000417050.1:n.171+377995C>A
|
|
ENST00000492288.1:n.441C>A
|
|
|
NM_000397.3:c.1016C>A , LRG_53t1:c.1016C>A
|
NP_000388.2:p.Pro339His
|
|
XM_011543890.1:c.710C>A
|
XP_011542192.1:p.Pro237His
|
|
NM_000397.4:c.1016C>A
MANE Select
|
NP_000388.2:p.Pro339His
|
|