ENST00000399503.4:c.2585A>C
MANE Select
|
ENSP00000382423.3:p.Glu862Ala
|
|
ENST00000399503.3:c.2585A>C
|
ENSP00000382423.3:p.Glu862Ala
|
|
NM_005921.1:c.2585A>C
|
NP_005912.1:p.Glu862Ala
|
|
XM_005248519.3:c.2207A>C
|
XP_005248576.2:p.Glu736Ala
|
|
XM_011543406.1:c.2330A>C
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XP_011541708.1:p.Glu777Ala
|
|
XM_011543407.1:c.2306A>C
|
XP_011541709.1:p.Glu769Ala
|
|
XM_011543408.1:c.2585A>C
|
XP_011541710.1:p.Glu862Ala
|
|
XM_017009484.1:c.2174A>C
|
XP_016864973.1:p.Glu725Ala
|
|
XM_017009485.1:c.2096A>C
|
XP_016864974.1:p.Glu699Ala
|
|
XR_001742068.2:n.2616A>C
|
|
|
NM_005921.2:c.2585A>C
MANE Select
|
NP_005912.1:p.Glu862Ala
|
|