ENST00000496887.7:c.441G>T
|
ENSP00000434560.2:p.Gln147His
|
|
ENST00000646564.2:c.478-11404G>T
|
ENSP00000495806.2:n.478-11404G>T
|
|
ENST00000155840.12:c.702G>T
MANE Select
|
ENSP00000155840.2:p.Gln234His
|
|
ENST00000335475.6:c.321G>T
|
ENSP00000334497.5:p.Gln107His
|
|
ENST00000646564.1:c.124-11404G>T
|
ENSP00000495806.1:n.124-11404G>T
|
|
ENST00000155840.9:c.702G>T
|
ENSP00000155840.2:p.Gln234His
|
|
ENST00000335475.5:c.321G>T
|
ENSP00000334497.5:p.Gln107His
|
|
ENST00000496887.6:c.441G>T
|
ENSP00000434560.1:p.Gln147His
|
|
NM_000218.2:c.702G>T , LRG_287t1:c.702G>T
|
NP_000209.2:p.Gln234His
|
|
NM_181798.1:c.321G>T , LRG_287t2:c.321G>T
|
NP_861463.1:p.Gln107His
|
|
NM_000218.3:c.702G>T
MANE Select
|
NP_000209.2:p.Gln234His
|
|