ENST00000495986.2:n.493G>T
|
|
|
ENST00000682365.1:n.1684G>T
|
|
|
ENST00000684251.1:n.193G>T
|
|
|
ENST00000684503.1:n.514G>T
|
|
|
ENST00000684692.1:c.349G>T
|
ENSP00000506792.1:p.Val117Phe
|
|
ENST00000168216.11:c.349G>T
MANE Select
|
ENSP00000168216.6:p.Val117Phe
|
|
ENST00000168216.10:c.349G>T
|
ENSP00000168216.6:p.Val117Phe
|
|
ENST00000375298.4:c.349G>T
|
ENSP00000364447.4:p.Val117Phe
|
|
ENST00000375304.9:c.349G>T
|
ENSP00000364453.5:p.Val117Phe
|
|
ENST00000477706.1:n.68G>T
|
|
|
ENST00000495986.1:n.481G>T
|
|
|
NM_001037811.2:c.349G>T , LRG_450t2:c.349G>T
|
NP_001032900.1:p.Val117Phe
|
|
NM_004493.2:c.349G>T , LRG_450t1:c.349G>T
|
NP_004484.1:p.Val117Phe
|
|
NM_004493.3:c.349G>T
MANE Select
|
NP_004484.1:p.Val117Phe
|
|