ENST00000260210.5:c.1850A>C
MANE Select
|
ENSP00000260210.3:p.Glu617Ala
|
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ENST00000260210.4:c.1850A>C
|
ENSP00000260210.3:p.Glu617Ala
|
|
ENST00000375445.7:c.1448A>C
|
ENSP00000364594.3:p.Glu483Ala
|
|
ENST00000419189.1:c.625A>C
|
|
|
NM_001159736.1:c.1448A>C
|
NP_001153208.1:p.Glu483Ala
|
|
NM_032725.3:c.1850A>C
|
NP_116114.1:p.Glu617Ala
|
|
XM_011543035.1:c.1751A>C
|
XP_011541337.1:p.Glu584Ala
|
|
XM_011543035.2:c.1751A>C
|
XP_011541337.1:p.Glu584Ala
|
|
NM_032725.4:c.1850A>C
MANE Select
|
NP_116114.1:p.Glu617Ala
|
|
NM_001159736.2:c.1448A>C
|
NP_001153208.1:p.Glu483Ala
|
|