ENST00000333213.11:c.1522G>C
MANE Select
|
ENSP00000327487.6:p.Gly508Arg
|
|
ENST00000434205.8:c.1219G>C
|
ENSP00000406559.4:p.Gly407Arg
|
|
ENST00000545228.3:c.*21G>C
|
ENSP00000438169.3:n.*21G>C
|
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ENST00000577197.2:n.720G>C
|
|
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ENST00000579449.2:n.2262G>C
|
|
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ENST00000580013.6:n.2666G>C
|
|
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ENST00000679370.1:n.3044G>C
|
|
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ENST00000679429.1:c.*980G>C
|
ENSP00000505403.1:n.*980G>C
|
|
ENST00000679443.1:n.1591G>C
|
|
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ENST00000679782.1:c.*221G>C
|
ENSP00000505995.1:n.*221G>C
|
|
ENST00000679919.1:n.1793G>C
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|
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ENST00000679928.1:c.*2074G>C
|
ENSP00000506071.1:n.*2074G>C
|
|
ENST00000680528.1:n.2488G>C
|
|
|
ENST00000680999.1:c.1735G>C
|
ENSP00000504984.1:p.Gly579Arg
|
|
ENST00000681282.1:c.*1709G>C
|
ENSP00000506339.1:n.*1709G>C
|
|
ENST00000333213.10:c.1522G>C
|
ENSP00000327487.6:p.Gly508Arg
|
|
ENST00000545228.2:c.799G>C
|
|
|
ENST00000577197.1:n.270G>C
|
|
|
ENST00000579449.1:n.719G>C
|
|
|
NM_207346.2:c.1522G>C
|
NP_997229.2:p.Gly508Arg
|
|
XM_005257229.2:c.*21G>C
|
XP_005257286.1:n.*21G>C
|
|
XM_006721821.2:c.*21G>C
|
XP_006721884.1:n.*21G>C
|
|
XM_011524616.1:c.*21G>C
|
XP_011522918.1:n.*21G>C
|
|
XM_011524618.1:c.1405G>C
|
XP_011522920.1:p.Gly469Arg
|
|
XR_243646.2:n.1754G>C
|
|
|
XM_005257229.4:c.*21G>C
|
XP_005257286.1:n.*21G>C
|
|
XR_001753015.1:n.45C>G
|
|
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XR_001753016.1:n.46C>G
|
|
|
XR_243646.4:n.1760G>C
|
|
|
NM_207346.3:c.1522G>C
MANE Select
|
NP_997229.2:p.Gly508Arg
|
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