ENST00000463045.3:c.351A>T
|
ENSP00000481376.2:p.Ile117=
|
|
ENST00000491274.6:c.480A>T
|
ENSP00000480482.2:p.Ile160=
|
|
ENST00000375499.8:c.522A>T
MANE Select
|
ENSP00000364649.3:p.Ile174=
|
|
ENST00000375499.7:c.522A>T
|
ENSP00000364649.3:p.Ile174=
|
|
ENST00000463045.2:c.351A>T
|
ENSP00000481376.1:p.Ile117=
|
|
ENST00000475506.1:n.439A>T
|
|
|
ENST00000485515.5:n.456A>T
|
|
|
ENST00000491274.5:c.480A>T
|
ENSP00000480482.1:p.Ile160=
|
|
NM_003000.2:c.522A>T , LRG_316t1:c.522A>T
|
NP_002991.2:p.Ile174=
|
|
NM_003000.3:c.522A>T
MANE Select
|
NP_002991.2:p.Ile174=
|
|