ENST00000255030.9:c.388G>C
MANE Select
|
ENSP00000255030.5:p.Asp130His
|
|
ENST00000368110.1:c.194-172G>C
|
ENSP00000357091.1:n.194-172G>C
|
|
ENST00000368111.5:c.194-172G>C
|
ENSP00000357092.1:n.194-172G>C
|
|
ENST00000368112.5:c.197+191G>C
|
ENSP00000357093.1:n.197+191G>C
|
|
ENST00000437342.1:c.-147G>C
|
ENSP00000402788.1:n.-147G>C
|
|
ENST00000489317.1:n.74+195G>C
|
|
|
NM_000567.2:c.388G>C
|
NP_000558.2:p.Asp130His
|
|
XM_011509207.1:c.388G>C
|
XP_011507509.1:p.Asp130His
|
|
NM_001329057.1:c.388G>C
|
NP_001315986.1:p.Asp130His
|
|
NM_001329058.1:c.197+191G>C
|
NP_001315987.1:n.197+191G>C
|
|
NM_000567.3:c.388G>C
MANE Select
|
NP_000558.2:p.Asp130His
|
|
NM_001329057.2:c.388G>C
|
NP_001315986.1:p.Asp130His
|
|
NM_001329058.2:c.197+191G>C
|
NP_001315987.1:n.197+191G>C
|
|
NM_001382703.1:c.194-172G>C
|
NP_001369632.1:n.194-172G>C
|
|