ENST00000542664.4:c.1195T>C
MANE Select
|
ENSP00000437737.1:p.Tyr399His
|
|
ENST00000543956.5:c.706T>C
|
ENSP00000441861.2:p.Tyr236His
|
|
ENST00000378688.8:c.1195T>C
|
ENSP00000367959.3:p.Tyr399His
|
|
ENST00000542664.3:c.1195T>C
|
ENSP00000437737.1:p.Tyr399His
|
|
ENST00000543956.4:c.943T>C
|
ENSP00000441861.1:p.Tyr315His
|
|
NM_000621.4:c.1195T>C
|
NP_000612.1:p.Tyr399His
|
|
NM_001165947.2:c.943T>C
|
NP_001159419.1:p.Tyr315His
|
|
NM_000621.5:c.1195T>C
MANE Select
|
NP_000612.1:p.Tyr399His
|
|
NM_001165947.5:c.706T>C
|
NP_001159419.2:p.Tyr236His
|
|
NM_001378924.1:c.1195T>C
|
NP_001365853.1:p.Tyr399His
|
|