ENST00000262493.12:c.952G>C
MANE Select
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ENSP00000262493.6:p.Glu318Gln
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ENST00000562316.6:c.545-1163G>C
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ENSP00000457238.2:n.545-1163G>C
|
|
ENST00000564727.2:c.256G>C
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ENSP00000454971.2:p.Glu86Gln
|
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ENST00000568375.2:c.190G>C
|
|
|
ENST00000638210.1:n.1252G>C
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|
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ENST00000638705.1:c.952G>C
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ENSP00000491223.1:p.Glu318Gln
|
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ENST00000638836.1:n.862G>C
|
|
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ENST00000639251.1:n.853G>C
|
|
|
ENST00000639268.1:c.587G>C
|
|
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ENST00000639341.1:c.477G>C
|
|
|
ENST00000639770.1:c.990G>C
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ENSP00000491999.1:n.990G>C
|
|
ENST00000640390.1:n.882G>C
|
|
|
ENST00000640469.1:c.316G>C
|
ENSP00000491875.1:p.Glu106Gln
|
|
ENST00000640560.1:n.728G>C
|
|
|
ENST00000640893.1:c.*350G>C
|
ENSP00000492677.1:n.*350G>C
|
|
ENST00000262493.10:c.952G>C
|
ENSP00000262493.6:p.Glu318Gln
|
|
ENST00000564727.1:c.172G>C
|
ENSP00000454971.1:p.Glu58Gln
|
|
ENST00000568375.1:n.190G>C
|
|
|
NM_020988.2:c.952G>C
|
NP_066268.1:p.Glu318Gln
|
|
XM_011523003.1:c.826G>C
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XP_011521305.1:p.Glu276Gln
|
|
XM_011523003.3:c.826G>C
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XP_011521305.1:p.Glu276Gln
|
|
NM_020988.3:c.952G>C
MANE Select
|
NP_066268.1:p.Glu318Gln
|
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