ENST00000700555.2:n.194A>T
|
|
|
ENST00000700559.2:c.1682A>T
|
ENSP00000515065.2:p.Glu561Val
|
|
ENST00000700563.2:c.1682A>T
|
ENSP00000515066.2:p.Glu561Val
|
|
ENST00000546498.2:n.369A>T
|
|
|
ENST00000700555.1:c.122A>T
|
ENSP00000515062.1:p.Glu41Val
|
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ENST00000700556.1:c.153A>T
|
|
|
ENST00000700559.1:c.897A>T
|
|
|
ENST00000700560.1:n.897A>T
|
|
|
ENST00000700561.1:n.1023A>T
|
|
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ENST00000700563.1:c.1636A>T
|
|
|
ENST00000700564.1:n.1686A>T
|
|
|
ENST00000070846.11:c.1814A>T
|
ENSP00000070846.6:p.Glu605Val
|
|
ENST00000340811.9:c.1682A>T
MANE Select
|
ENSP00000342800.5:p.Glu561Val
|
|
ENST00000070846.10:c.1814A>T
|
ENSP00000070846.6:p.Glu605Val
|
|
ENST00000340811.8:c.1682A>T
|
ENSP00000342800.4:p.Glu561Val
|
|
ENST00000546498.1:n.369A>T
|
|
|
ENST00000552612.5:n.103A>T
|
|
|
ENST00000613243.1:c.1814A>T
|
ENSP00000478295.1:p.Glu605Val
|
|
NM_001005242.2:c.1682A>T
|
NP_001005242.2:p.Glu561Val
|
|
NM_004572.3:c.1814A>T , LRG_398t1:c.1814A>T
|
NP_004563.2:p.Glu605Val
|
|
NM_001005242.3:c.1682A>T
MANE Select
|
NP_001005242.2:p.Glu561Val
|
|
NM_004572.4:c.1814A>T
|
NP_004563.2:p.Glu605Val
|
|