ENST00000700555.2:n.251A>T
|
|
|
ENST00000700559.2:c.1739A>T
|
ENSP00000515065.2:p.Glu580Val
|
|
ENST00000700563.2:c.1739A>T
|
ENSP00000515066.2:p.Glu580Val
|
|
ENST00000546498.2:n.426A>T
|
|
|
ENST00000700555.1:c.179A>T
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ENSP00000515062.1:p.Glu60Val
|
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ENST00000700556.1:c.210A>T
|
|
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ENST00000700559.1:c.954A>T
|
|
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ENST00000700560.1:n.954A>T
|
|
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ENST00000700561.1:n.1080A>T
|
|
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ENST00000700563.1:c.1693A>T
|
|
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ENST00000700564.1:n.1743A>T
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|
|
ENST00000070846.11:c.1871A>T
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ENSP00000070846.6:p.Glu624Val
|
|
ENST00000340811.9:c.1739A>T
MANE Select
|
ENSP00000342800.5:p.Glu580Val
|
|
ENST00000070846.10:c.1871A>T
|
ENSP00000070846.6:p.Glu624Val
|
|
ENST00000340811.8:c.1739A>T
|
ENSP00000342800.4:p.Glu580Val
|
|
ENST00000546498.1:n.426A>T
|
|
|
ENST00000552612.5:n.160A>T
|
|
|
ENST00000613243.1:c.1871A>T
|
ENSP00000478295.1:p.Glu624Val
|
|
NM_001005242.2:c.1739A>T
|
NP_001005242.2:p.Glu580Val
|
|
NM_004572.3:c.1871A>T , LRG_398t1:c.1871A>T
|
NP_004563.2:p.Glu624Val
|
|
NM_001005242.3:c.1739A>T
MANE Select
|
NP_001005242.2:p.Glu580Val
|
|
NM_004572.4:c.1871A>T
|
NP_004563.2:p.Glu624Val
|
|