ENST00000696142.1:c.*192C>A
|
ENSP00000512434.1:n.*192C>A
|
|
ENST00000696143.1:c.651C>A
|
ENSP00000512435.1:n.651C>A
|
|
ENST00000696153.1:c.626C>A
|
ENSP00000512444.1:p.Pro209His
|
|
ENST00000256474.3:c.515C>A
MANE Select
|
ENSP00000256474.3:p.Pro172His
|
|
ENST00000256474.2:c.515C>A
|
ENSP00000256474.2:p.Pro172His
|
|
ENST00000345392.2:c.392C>A
|
ENSP00000344757.2:p.Pro131His
|
|
ENST00000477538.1:n.651C>A
|
|
|
NM_000551.3:c.515C>A , LRG_322t1:c.515C>A
|
NP_000542.1:p.Pro172His
|
|
NM_198156.2:c.392C>A
|
NP_937799.1:p.Pro131His
|
|
NM_001354723.1:c.*69C>A
|
NP_001341652.1:n.*69C>A
|
|
NM_000551.4:c.515C>A
MANE Select
|
NP_000542.1:p.Pro172His
|
|
NM_001354723.2:c.*69C>A
|
NP_001341652.1:n.*69C>A
|
|
NM_198156.3:c.392C>A
|
NP_937799.1:p.Pro131His
|
|