ENST00000324856.13:c.5362A>C
MANE Select
|
ENSP00000320485.7:p.Ile1788Leu
|
|
ENST00000374152.7:c.4213A>C
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ENSP00000363267.2:p.Ile1405Leu
|
|
ENST00000430799.7:c.4210A>C
|
ENSP00000390317.3:p.Ile1404Leu
|
|
ENST00000466382.2:c.779A>C
|
|
|
ENST00000636219.1:c.4216A>C
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ENSP00000489842.1:p.Ile1406Leu
|
|
ENST00000637788.1:n.1162A>C
|
|
|
ENST00000324856.11:c.5362A>C
|
ENSP00000320485.7:p.Ile1788Leu
|
|
ENST00000374152.6:c.4213A>C
|
ENSP00000363267.2:p.Ile1405Leu
|
|
ENST00000430799.6:c.2051A>C
|
|
|
ENST00000457599.6:c.4711A>C
|
ENSP00000387636.2:p.Ile1571Leu
|
|
ENST00000466382.1:c.779A>C
|
|
|
ENST00000532781.1:c.860A>C
|
|
|
NM_006015.4:c.5362A>C , LRG_875t1:c.5362A>C
|
NP_006006.3:p.Ile1788Leu
|
|
NM_139135.2:c.4711A>C
|
NP_624361.1:p.Ile1571Leu
|
|
NM_006015.5:c.5362A>C
|
NP_006006.3:p.Ile1788Leu
|
|
NM_139135.3:c.4711A>C
|
NP_624361.1:p.Ile1571Leu
|
|
NM_006015.6:c.5362A>C
MANE Select
|
NP_006006.3:p.Ile1788Leu
|
|
NM_139135.4:c.4711A>C
|
NP_624361.1:p.Ile1571Leu
|
|