ENST00000302068.9:c.1091A>T
MANE Select
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ENSP00000306099.4:p.Glu364Val
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|
ENST00000302068.8:c.1091A>T
|
ENSP00000306099.4:p.Glu364Val
|
|
ENST00000502545.5:n.939+339A>T
|
|
|
ENST00000509493.1:c.434A>T
|
ENSP00000426757.1:p.Glu145Val
|
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NM_001184741.1:c.914A>T
|
NP_001171670.1:p.Glu305Val
|
|
NM_005141.4:c.1091A>T , LRG_558t1:c.1091A>T
|
NP_005132.2:p.Glu364Val
|
|
NM_001382759.1:c.959A>T
|
NP_001369688.1:p.Glu320Val
|
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NM_001382760.1:c.1091A>T
|
NP_001369689.1:p.Glu364Val
|
|
NM_001382761.1:c.1091A>T
|
NP_001369690.1:p.Glu364Val
|
|
NM_001382762.1:c.791A>T
|
NP_001369691.1:p.Glu264Val
|
|
NM_001382763.1:c.1082A>T
|
NP_001369692.1:p.Glu361Val
|
|
NM_001382764.1:c.1080+11A>T
|
NP_001369693.1:n.1080+11A>T
|
|
NM_001382765.1:c.1091A>T
|
NP_001369694.1:p.Glu364Val
|
|
NM_005141.5:c.1091A>T
MANE Select
|
NP_005132.2:p.Glu364Val
|
|