ENST00000700555.2:n.554A>T
|
|
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ENST00000700557.2:n.143A>T
|
|
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ENST00000700559.2:c.2051A>T
|
ENSP00000515065.2:p.Glu684Val
|
|
ENST00000546498.2:n.738A>T
|
|
|
ENST00000549461.2:n.590A>T
|
|
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ENST00000700555.1:c.482A>T
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ENSP00000515062.1:p.Glu161Val
|
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ENST00000700556.1:c.522A>T
|
|
|
ENST00000700557.1:c.62A>T
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ENSP00000515064.1:p.Glu21Val
|
|
ENST00000700558.1:n.265A>T
|
|
|
ENST00000700559.1:c.1266A>T
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|
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ENST00000700560.1:n.1266A>T
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|
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ENST00000700561.1:n.1392A>T
|
|
|
ENST00000070846.11:c.2183A>T
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ENSP00000070846.6:p.Glu728Val
|
|
ENST00000340811.9:c.2051A>T
MANE Select
|
ENSP00000342800.5:p.Glu684Val
|
|
ENST00000070846.10:c.2183A>T
|
ENSP00000070846.6:p.Glu728Val
|
|
ENST00000340811.8:c.2051A>T
|
ENSP00000342800.4:p.Glu684Val
|
|
ENST00000549461.1:n.497A>T
|
|
|
ENST00000613243.1:c.2183A>T
|
ENSP00000478295.1:p.Glu728Val
|
|
NM_001005242.2:c.2051A>T
|
NP_001005242.2:p.Glu684Val
|
|
NM_004572.3:c.2183A>T , LRG_398t1:c.2183A>T
|
NP_004563.2:p.Glu728Val
|
|
NM_001005242.3:c.2051A>T
MANE Select
|
NP_001005242.2:p.Glu684Val
|
|
NM_004572.4:c.2183A>T
|
NP_004563.2:p.Glu728Val
|
|