ENST00000399820.8:c.2541A>C
MANE Select
|
ENSP00000382717.3:p.Gly847=
|
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ENST00000399820.7:c.2541A>C
|
ENSP00000382717.3:p.Gly847=
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|
ENST00000506869.5:c.*2122A>C
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ENSP00000424319.1:n.*2122A>C
|
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ENST00000512095.5:n.1539A>C
|
|
|
NM_025132.3:c.2541A>C
|
NP_079408.3:p.Gly847=
|
|
XM_011513724.1:c.2553A>C
|
XP_011512026.1:p.Gly851=
|
|
XM_011513725.1:c.2487A>C
|
XP_011512027.1:p.Gly829=
|
|
XM_011513726.1:c.2073A>C
|
XP_011512028.1:p.Gly691=
|
|
XM_011513727.1:c.2073A>C
|
XP_011512029.1:p.Gly691=
|
|
XM_011513728.1:c.2061A>C
|
XP_011512030.1:p.Gly687=
|
|
XM_011513729.1:c.2553A>C
|
XP_011512031.1:p.Gly851=
|
|
XR_925155.1:n.2617A>C
|
|
|
NM_001317924.1:c.2061A>C
|
NP_001304853.1:p.Gly687=
|
|
XM_011513725.2:c.2487A>C
|
XP_011512027.1:p.Gly829=
|
|
XM_011513726.3:c.2073A>C
|
XP_011512028.1:p.Gly691=
|
|
XM_017008501.1:c.2061A>C
|
XP_016863990.1:p.Gly687=
|
|
XR_001741306.1:n.2617A>C
|
|
|
XR_001741307.1:n.2605A>C
|
|
|
XR_001741308.1:n.2617A>C
|
|
|
XR_001741309.1:n.2605A>C
|
|
|
XR_001741310.1:n.2605A>C
|
|
|
XR_001741311.2:n.2454A>C
|
|
|
NM_025132.4:c.2541A>C
MANE Select
|
NP_079408.3:p.Gly847=
|
|
NM_001317924.2:c.2061A>C
|
NP_001304853.1:p.Gly687=
|
|