ENST00000696142.1:c.*236G>C
|
ENSP00000512434.1:n.*236G>C
|
|
ENST00000696143.1:c.695G>C
|
ENSP00000512435.1:n.695G>C
|
|
ENST00000696153.1:c.670G>C
|
ENSP00000512444.1:p.Asp224His
|
|
ENST00000256474.3:c.559G>C
MANE Select
|
ENSP00000256474.3:p.Asp187His
|
|
ENST00000256474.2:c.559G>C
|
ENSP00000256474.2:p.Asp187His
|
|
ENST00000345392.2:c.436G>C
|
ENSP00000344757.2:p.Asp146His
|
|
ENST00000477538.1:n.695G>C
|
|
|
NM_000551.3:c.559G>C , LRG_322t1:c.559G>C
|
NP_000542.1:p.Asp187His
|
|
NM_198156.2:c.436G>C
|
NP_937799.1:p.Asp146His
|
|
NM_001354723.1:c.*113G>C
|
NP_001341652.1:n.*113G>C
|
|
NM_000551.4:c.559G>C
MANE Select
|
NP_000542.1:p.Asp187His
|
|
NM_001354723.2:c.*113G>C
|
NP_001341652.1:n.*113G>C
|
|
NM_198156.3:c.436G>C
|
NP_937799.1:p.Asp146His
|
|