ENST00000526008.6:c.538C=
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ENSP00000513006.1:p.Arg180=
|
|
ENST00000458235.7:c.538C=
MANE Select
|
ENSP00000391676.1:p.Arg180=
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|
ENST00000458235.5:c.538C=
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ENSP00000391676.1:p.Arg180=
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ENST00000526008.5:n.638C=
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|
|
ENST00000527031.5:n.628C=
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|
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ENST00000527670.5:c.538C=
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ENSP00000432511.1:p.Arg180=
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|
ENST00000528293.1:n.553C=
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|
|
ENST00000534444.1:c.538C=
|
ENSP00000436421.1:p.Arg180=
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|
NM_000215.3:c.538C= , LRG_77t1:c.538C=
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NP_000206.2:p.Arg180=
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|
XM_005259896.2:c.667C=
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XP_005259953.1:p.Arg223=
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|
XM_006722745.2:c.538C=
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XP_006722808.1:p.Arg180=
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|
XM_011527990.1:c.667C=
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XP_011526292.1:p.Arg223=
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|
XM_011527991.1:c.667C=
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XP_011526293.1:p.Arg223=
|
|
XR_430137.2:n.677C=
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|
|
XM_005259896.3:c.667C=
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XP_005259953.1:p.Arg223=
|
|
XM_011527991.2:c.667C=
|
XP_011526293.1:p.Arg223=
|
|
NM_000215.4:c.538C=
MANE Select
|
NP_000206.2:p.Arg180=
|
|