ENST00000340855.11:c.621G>C
MANE Select
|
ENSP00000339801.6:p.Gln207His
|
|
ENST00000651111.1:c.-13G>C
|
ENSP00000498395.1:n.-13G>C
|
|
ENST00000340855.10:c.621G>C
|
ENSP00000339801.6:p.Gln207His
|
|
ENST00000370441.8:c.621G>C
|
ENSP00000359470.4:p.Gln207His
|
|
ENST00000422081.6:c.-13G>C
|
ENSP00000477056.1:n.-13G>C
|
|
ENST00000441880.1:n.114-11096G>C
|
|
|
ENST00000464251.5:c.547G>C
|
ENSP00000428980.1:n.547G>C
|
|
ENST00000466019.1:n.73G>C
|
|
|
ENST00000466323.5:c.621G>C
|
ENSP00000418264.1:p.Gln207His
|
|
ENST00000490775.5:n.406G>C
|
|
|
ENST00000523759.5:n.735G>C
|
|
|
NM_000202.6:c.621G>C
|
NP_000193.1:p.Gln207His
|
|
NM_001166550.2:c.351G>C
|
NP_001160022.1:p.Gln117His
|
|
NM_006123.4:c.621G>C
|
NP_006114.1:p.Gln207His
|
|
NR_104128.1:n.838G>C
|
|
|
NM_000202.7:c.621G>C
|
NP_000193.1:p.Gln207His
|
|
NM_001166550.3:c.351G>C
|
NP_001160022.1:p.Gln117His
|
|
NM_000202.8:c.621G>C
MANE Select
|
NP_000193.1:p.Gln207His
|
|
NM_001166550.4:c.351G>C
|
NP_001160022.1:p.Gln117His
|
|
NM_006123.5:c.621G>C
|
NP_006114.1:p.Gln207His
|
|
NR_104128.2:n.790G>C
|
|
|