ENST00000693473.1:c.2649A>C
|
|
|
ENST00000371113.9:c.2532A>C
MANE Select
|
ENSP00000360154.4:p.Arg844=
|
|
ENST00000646010.1:c.2580A>C
|
|
|
ENST00000646914.1:c.1837A>C
|
|
|
ENST00000647245.1:c.2083A>C
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|
|
ENST00000357121.5:c.2508A>C
|
ENSP00000349635.5:p.Arg836=
|
|
ENST00000371113.8:c.2532A>C
|
ENSP00000360154.4:p.Arg844=
|
|
ENST00000463271.1:n.319A>C
|
|
|
NM_000276.3:c.2532A>C
|
NP_000267.2:p.Arg844=
|
|
NM_001587.3:c.2508A>C
|
NP_001578.2:p.Arg836=
|
|
XM_005262422.1:c.2061A>C
|
XP_005262479.1:p.Arg687=
|
|
XM_011531342.1:c.2535A>C
|
XP_011529644.1:p.Arg845=
|
|
XM_011531343.1:c.2511A>C
|
XP_011529645.1:p.Arg837=
|
|
XM_011531344.1:c.2388A>C
|
XP_011529646.1:p.Arg796=
|
|
XM_011531345.1:c.2388A>C
|
XP_011529647.1:p.Arg796=
|
|
NM_001318784.1:c.2535A>C
|
NP_001305713.1:p.Arg845=
|
|
XM_005262422.2:c.2061A>C
|
XP_005262479.1:p.Arg687=
|
|
XM_011531344.3:c.2388A>C
|
XP_011529646.1:p.Arg796=
|
|
XM_011531345.3:c.2388A>C
|
XP_011529647.1:p.Arg796=
|
|
NM_000276.4:c.2532A>C
MANE Select
|
NP_000267.2:p.Arg844=
|
|
NM_001318784.2:c.2535A>C
|
NP_001305713.1:p.Arg845=
|
|
NM_001587.4:c.2508A>C
|
NP_001578.2:p.Arg836=
|
|