ENST00000302068.9:c.1026A=
MANE Select
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ENSP00000306099.4:p.Ile342=
|
|
ENST00000302068.8:c.1026A=
|
ENSP00000306099.4:p.Ile342=
|
|
ENST00000502545.5:n.939+274A=
|
|
|
ENST00000509493.1:c.369A=
|
ENSP00000426757.1:p.Ile123=
|
|
NM_001184741.1:c.849A=
|
NP_001171670.1:p.Ile283=
|
|
NM_005141.4:c.1026A= , LRG_558t1:c.1026A=
|
NP_005132.2:p.Ile342=
|
|
NM_001382759.1:c.894A=
|
NP_001369688.1:p.Ile298=
|
|
NM_001382760.1:c.1026A=
|
NP_001369689.1:p.Ile342=
|
|
NM_001382761.1:c.1026A=
|
NP_001369690.1:p.Ile342=
|
|
NM_001382762.1:c.746-20A=
|
NP_001369691.1:n.746-20A=
|
|
NM_001382763.1:c.1017A=
|
NP_001369692.1:p.Ile339=
|
|
NM_001382764.1:c.1026A=
|
NP_001369693.1:p.Ile342=
|
|
NM_001382765.1:c.1026A=
|
NP_001369694.1:p.Ile342=
|
|
NM_005141.5:c.1026A=
MANE Select
|
NP_005132.2:p.Ile342=
|
|