ENST00000348974.5:c.769G>T
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ENSP00000330021.7:p.Val257Phe
|
|
ENST00000394236.9:c.769G>T
MANE Select
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ENSP00000377783.3:p.Val257Phe
|
|
ENST00000407433.6:c.724G>T
|
ENSP00000385794.2:p.Val242Phe
|
|
ENST00000647936.1:c.769G>T
|
ENSP00000496822.1:p.Val257Phe
|
|
ENST00000648381.1:n.937G>T
|
|
|
ENST00000648853.1:c.727G>T
|
ENSP00000497262.1:p.Val243Phe
|
|
ENST00000649103.1:c.868G>T
|
ENSP00000497962.1:n.868G>T
|
|
ENST00000650591.1:c.865G>T
|
ENSP00000497376.1:p.Val289Phe
|
|
ENST00000394236.7:c.769G>T
|
ENSP00000377783.3:p.Val257Phe
|
|
ENST00000407433.5:c.376G>T
|
ENSP00000385794.1:p.Val126Phe
|
|
NM_000313.3:c.769G>T , LRG_572t1:c.769G>T
|
NP_000304.2:p.Val257Phe
|
|
NM_001314077.1:c.865G>T , LRG_572t2:c.865G>T
|
NP_001301006.1:p.Val289Phe
|
|
NM_000313.4:c.769G>T
MANE Select
|
NP_000304.2:p.Val257Phe
|
|
NM_001314077.2:c.865G>T
|
NP_001301006.1:p.Val289Phe
|
|