ENST00000340855.11:c.1026T>C
MANE Select
|
ENSP00000339801.6:p.His342=
|
|
ENST00000651111.1:c.393T>C
|
ENSP00000498395.1:p.His131=
|
|
ENST00000340855.10:c.1026T>C
|
ENSP00000339801.6:p.His342=
|
|
ENST00000422081.6:c.393T>C
|
ENSP00000477056.1:p.His131=
|
|
ENST00000441880.1:n.133T>C
|
|
|
NM_000202.6:c.1026T>C
|
NP_000193.1:p.His342=
|
|
NM_001166550.2:c.756T>C
|
NP_001160022.1:p.His252=
|
|
NM_000202.7:c.1026T>C
|
NP_000193.1:p.His342=
|
|
NM_001166550.3:c.756T>C
|
NP_001160022.1:p.His252=
|
|
NM_000202.8:c.1026T>C
MANE Select
|
NP_000193.1:p.His342=
|
|
NM_001166550.4:c.756T>C
|
NP_001160022.1:p.His252=
|
|