ENST00000561514.3:c.2993A>C
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ENSP00000460666.3:p.Glu998Ala
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ENST00000565038.2:c.*468A>C
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ENSP00000459882.2:n.*468A>C
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ENST00000566069.6:c.2987A>C
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ENSP00000459237.2:p.Glu996Ala
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ENST00000697377.2:c.2831A>C
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ENSP00000513286.2:p.Glu944Ala
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ENST00000697379.2:c.2993A>C
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ENSP00000513287.2:p.Glu998Ala
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ENST00000561514.2:c.2102A>C
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ENSP00000460666.2:p.Glu701Ala
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ENST00000697374.1:c.2102A>C
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ENSP00000513284.1:p.Glu701Ala
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ENST00000697375.1:n.4334A>C
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ENST00000697376.1:c.2102A>C
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ENSP00000513285.1:p.Glu701Ala
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ENST00000697377.1:c.1940A>C
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ENSP00000513286.1:p.Glu647Ala
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ENST00000697378.1:n.3507A>C
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ENST00000697379.1:c.2102A>C
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ENSP00000513287.1:p.Glu701Ala
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ENST00000697380.1:n.2279A>C
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|
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ENST00000697381.1:n.1682A>C
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|
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ENST00000697382.1:c.2102A>C
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ENSP00000513288.1:p.Glu701Ala
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ENST00000697383.1:c.521A>C
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ENSP00000513289.1:p.Glu174Ala
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ENST00000261584.9:c.2987A>C
MANE Select
|
ENSP00000261584.4:p.Glu996Ala
|
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ENST00000261584.8:c.2987A>C
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ENSP00000261584.4:p.Glu996Ala
|
|
ENST00000568219.5:c.2102A>C
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ENSP00000454703.2:p.Glu701Ala
|
|
NM_024675.3:c.2987A>C , LRG_308t1:c.2987A>C
|
NP_078951.2:p.Glu996Ala
|
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XM_011545946.1:c.2993A>C
|
XP_011544248.1:p.Glu998Ala
|
|
XM_011545947.1:c.2993A>C
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XP_011544249.1:p.Glu998Ala
|
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XM_011545948.1:c.2102A>C
|
XP_011544250.1:p.Glu701Ala
|
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XR_950851.1:n.3783A>C
|
|
|
XM_011545946.2:c.2993A>C
|
XP_011544248.1:p.Glu998Ala
|
|
XM_011545947.2:c.2993A>C
|
XP_011544249.1:p.Glu998Ala
|
|
XM_011545948.2:c.2102A>C
|
XP_011544250.1:p.Glu701Ala
|
|
XM_017023671.1:c.2993A>C
|
XP_016879160.1:p.Glu998Ala
|
|
XM_017023672.2:c.2987A>C
|
XP_016879161.1:p.Glu996Ala
|
|
XM_017023673.2:c.2987A>C
|
XP_016879162.1:p.Glu996Ala
|
|
NM_024675.4:c.2987A>C
MANE Select
|
NP_078951.2:p.Glu996Ala
|
|