ENST00000261837.12:c.271G>C
MANE Select
|
ENSP00000261837.7:p.Gly91Arg
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ENST00000261837.11:c.271G>C
|
ENSP00000261837.7:p.Gly91Arg
|
|
ENST00000358784.11:c.145G>C
|
ENSP00000351635.7:p.Gly49Arg
|
|
ENST00000396335.8:c.145G>C
|
ENSP00000379626.4:p.Gly49Arg
|
|
ENST00000560075.1:n.302G>C
|
|
|
ENST00000560116.1:c.145G>C
|
ENSP00000453176.1:p.Gly49Arg
|
|
ENST00000561313.5:c.145G>C
|
ENSP00000454185.1:p.Gly49Arg
|
|
NM_006578.3:c.145G>C
|
NP_006569.1:p.Gly49Arg
|
|
NM_016194.3:c.271G>C
|
NP_057278.2:p.Gly91Arg
|
|
XM_011521162.1:c.145G>C
|
XP_011519464.1:p.Gly49Arg
|
|
XM_011521163.1:c.-12G>C
|
XP_011519465.1:n.-12G>C
|
|
XM_011521162.3:c.145G>C
|
XP_011519464.1:p.Gly49Arg
|
|
XM_011521163.3:c.-12G>C
|
XP_011519465.1:n.-12G>C
|
|
XR_001751060.2:n.223G>C
|
|
|
NM_006578.4:c.145G>C
|
NP_006569.1:p.Gly49Arg
|
|
NM_016194.4:c.271G>C
MANE Select
|
NP_057278.2:p.Gly91Arg
|
|
NM_001379343.1:c.-12G>C
|
NP_001366272.1:n.-12G>C
|
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